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I would like to be included in the K-Recruiting freelancer pool. This will give me the opportunity to receive further exciting offers. By being included in the freelancer pool, K-Recruiting GmbH (DE), K-Recruiting LP (US), K-Recruiting Schweiz AG (CH) and K-Recruiting Global AG (CH) will have access to my personal data and will be able to submit offers to me.

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<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">Einer unserer Pharma-Kunden in der Schweiz&nbsp;sucht aktuell Unterstützung als: &nbsp; Prozessmitarbeiter (M/W/D) &nbsp; Aufgaben:
<ul><li><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#32363a; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:left; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Ziel der Funktion:<br style="margin: 0px; padding: 0px; box-sizing: inherit; color: rgb(50, 54, 58); font-family: &quot;72&quot;, -apple-system, BlinkMacSystemFont, &quot;Segoe UI&quot;, Roboto, &quot;Helvetica Neue&quot;, Arial, sans-serif, &quot;Apple Color Emoji&quot;, &quot;Segoe UI Emoji&quot;, &quot;Segoe UI Symbol&quot;; font-size: 14px; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: left; text-indent: 0px; text-transform: none; white-space: normal; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; background-color: rgb(255, 255, 255); text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial;"><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#32363a; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:left; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Der Prozessmitarbeiter ist verantwortlich für die Überwachung der Assemblierung und Verpackungsanlagen von Autoinjektoren, Fertigspritzen und Safety Devices. Dabei hat er vollumfängliche Kenntnisse über die relevanten SOP's und Vorschriften (z.B. anlagespezifische SOP's, Hygienekonzept, GSU-Vorschriften, etc.). Aufgaben kann der Mitarbeiter selbstständig durchführen.</li><li><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#32363a; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:left; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Verantwortlich für die Überwachung der Anlage in seinem Bereich</li><li><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#32363a; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:left; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Verantwortlich für die konsequente Einhaltung der SOP`s, Daten Integrität, Hygiene und Sicherheitsvorschriften</li><li><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#32363a; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:left; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Sorgt für Sauberkeit, Hygiene und Ordnung im zu verantwortenden Bereich</li><li><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#32363a; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:left; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Umsetzen der 5S Standards</li><li><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#32363a; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:left; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Ausbildungsgerechte Mithilfe bei der Reinigung von Anlagen</li><li><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#32363a; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:left; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Korrekte, vollständige und fehlerfreie Eintragungen in Herstelldokumente, Log-Bücher und Dateneingabe</li><li><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#32363a; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:left; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Kennt den Stand Produktionsplan (z.B. Rückstand nach Produktionsplan)</li><li><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#32363a; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:left; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Durchführung der Startkontrolle (erste Kontrolle) und IPC</li><li><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#32363a; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:left; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Durchführung der Endkontrolle (Alter Auftrag, Bruch zählen)</li><li><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#32363a; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:left; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Führt die Funktionskontrolle seinem Bereich selbstständig durch</li><li><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#32363a; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:left; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Erkennen von Abweichungen</li><li><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#32363a; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:left; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Kann Dokumentationen in dem ihm zugeteilten Bereich im MES/Papier PAS durchführen</li><li><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#32363a; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:left; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Kann Störungen detailliert dem Technischen Support melden</li><li><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#32363a; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:left; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Kann Formatwechsel selbstständig durchführen</li><li><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#32363a; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:left; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Kann Störungen detailliert dem Technischen Support melden</li><li><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#32363a; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:left; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Kann Formatwechsel selbstständig durchführen</li></ul>
&nbsp;Qualifikation:
<ul><li><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#32363a; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:left; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Abgeschlossene in der Schweiz anerkannte Berufsausbildung</li><li><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#32363a; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:left; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Deutsch in Wort und Schrift</li><li><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#32363a; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:left; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Pharmaerfahrung von Vorteil</li></ul>
Rahmendaten: 
<ul><li style="list-style-position: inside;">Start: 01.10.2022</li><li style="list-style-position: inside;">Dauer: 31.12.2023</li><li style="list-style-position: inside;">Auslastung: 5 Tage die Woche</li><li style="list-style-position: inside;">Einsatzort: Stein, Schweiz</li></ul></div>

Prozessmitarbeiter

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">Einer unserer Medizintechnik-Kunden in Deutschland sucht aktuell freiberufliche Unterstützung als: &nbsp; Experte Hardwareentwicklung (m/w/d) &nbsp; Aufgaben:
<ul><li style="box-sizing: border-box; padding: 5px 0px 5px 20px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5; background: url(&quot;../img/list.png&quot;) 5px 10px no-repeat;">Sie ent­wick­eln ana­lo­ge und di­gi­ta­le Schal­tun­gen</li><li style="box-sizing: border-box; padding: 5px 0px 5px 20px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5; background: url(&quot;../img/list.png&quot;) 5px 10px no-repeat;">Sie er­stel­len elek­tri­sche Schalt­plä­ne/Lay­outs für hoch­in­te­grier­te Sys­te­me</li><li style="box-sizing: border-box; padding: 5px 0px 5px 20px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5; background: url(&quot;../img/list.png&quot;) 5px 10px no-repeat;">Sie haben Er­fah­rung in der Elek­tro­nik HW-Ent­wick­lung in den Be­rei­chen Schal­tungs­ent­wurf, Si­mu­la­ti­on und Lei­ter­plat­ten­lay­out</li><li style="box-sizing: border-box; padding: 5px 0px 5px 20px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5; background: url(&quot;../img/list.png&quot;) 5px 10px no-repeat;">Sie steuern die Nach­hal­ti­ge Do­ku­men­ta­ti­on der Ent­wick­lungs­er­geb­nis­se</li><li style="box-sizing: border-box; padding: 5px 0px 5px 20px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5; background: url(&quot;../img/list.png&quot;) 5px 10px no-repeat;">Sie steuern die Durch­füh­rung und Be­glei­tung von Va­li­die­rungs- und Qua­li­fi­zie­rungs­prü­fun­gen (in­tern und ex­tern)</li></ul>
&nbsp;Qualifikation:
<ul><li style="box-sizing: border-box; padding: 5px 0px 5px 20px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5; background: url(&quot;../img/list.png&quot;) 5px 10px no-repeat;">Sie ver­fü­gen über ein mit gutem Er­folg ab­ge­schlos­se­nes (Fach-) Hoch­schul­stu­di­um im Be­reich Elek­tro­tech­nik, Nach­rich­ten­tech­nik (oder ver­gleich­ba­rer Stu­di­en­gang)</li><li style="box-sizing: border-box; padding: 5px 0px 5px 20px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5; background: url(&quot;../img/list.png&quot;) 5px 10px no-repeat;">Sie haben über 3 Jahre Er­fah­rung in der Ent­wick­lung von Mi­xed-Si­gnal-Elek­tro­nik­ge­rä­ten oder vergleichbares&nbsp;</li><li style="box-sizing: border-box; padding: 5px 0px 5px 20px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5; background: url(&quot;../img/list.png&quot;) 5px 10px no-repeat;">Er­fah­rung im Um­gang mit La­bor­ge­rä­ten und Mess­in­stru­men­ten</li><li style="box-sizing: border-box; padding: 5px 0px 5px 20px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5; background: url(&quot;../img/list.png&quot;) 5px 10px no-repeat;">Er­fah­rung im De­bug­ging von Lei­ter­plat­ten-Bau­grup­pen, ein­schlie­ß­lich Löten von SMD-Bau­tei­len</li><li style="box-sizing: border-box; padding: 5px 0px 5px 20px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5; background: url(&quot;../img/list.png&quot;) 5px 10px no-repeat;">Er­fah­rung in der Er­stel­lung von Lay­outs be­züg­lich High-Speed-In­ter­faces, Mi­kro­con­trol­ler und Pro­zes­so­ren</li><li style="box-sizing: border-box; padding: 5px 0px 5px 20px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5; background: url(&quot;../img/list.png&quot;) 5px 10px no-repeat;">Sie haben einen si­che­ren Um­gang mit min­des­tens einem E-CAD-Pro­gramm</li><li style="box-sizing: border-box; padding: 5px 0px 5px 20px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5; background: url(&quot;../img/list.png&quot;) 5px 10px no-repeat;">Sie ken­nen sich in ent­wick­lungs­be­glei­ten­den The­men­fel­dern wie EMV- und Um­welt­an­for­de­run­gen gut aus</li><li style="box-sizing: border-box; padding: 5px 0px 5px 20px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5; background: url(&quot;../img/list.png&quot;) 5px 10px no-repeat;">Gute Sprach­kennt­nis­se in Deutsch und wer­den vor­aus­ge­setzt sowie sehr gute Eng­lisch­kennt­nis­se in Wort und Schrift</li><li style="box-sizing: border-box; padding: 5px 0px 5px 20px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5; background: url(&quot;../img/list.png&quot;) 5px 10px no-repeat;">Team­fä­hig­keit, Um­set­zungs­stär­ke und Ziel­ori­en­tie­rung, ef­fi­zi­en­tes Selbst­ma­nage­ment und ein hohes Maß an Zu­ver­läs­sig­keit</li><li style="box-sizing: border-box; padding: 5px 0px 5px 20px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5; background: url(&quot;../img/list.png&quot;) 5px 10px no-repeat;">Nice to have: Er­fah­rung mit Ge­rä­ten der Leis­tungs­elek­tro­nik</li><li style="box-sizing: border-box; padding: 5px 0px 5px 20px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5; background: url(&quot;../img/list.png&quot;) 5px 10px no-repeat;">Nice to have: Er­fah­rung mit dem Pro­gramm Al­ti­um De­si­gner</li><li style="box-sizing: border-box; padding: 5px 0px 5px 20px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5; background: url(&quot;../img/list.png&quot;) 5px 10px no-repeat;">&nbsp;</li></ul>
Rahmendaten: Start: sofort&nbsp; Dauer: 6 Monate Auslastung: 5 Tage die Woche Einsatzort: Baden-Württemberg
&nbsp;
&nbsp;
&nbsp;
One of our XXXX clients in Germany is currently looking for freelance support as:
&nbsp;
XXX (M/W/D) &nbsp; Tasks:
<ul><li>XX</li></ul>
&nbsp;Qualification:
<ul><li>XXX</li></ul>
Requirements: Start: XX Duration: XX months Capacity: XX days per week Location: XX</div>

Ingenieur in der Hardwareentwicklung (m/w/d)

<div data-wrapper="true" style="font-size:10pt;font-family:Arial;">Einer unserer Medizintechnik-Kunden in Deutschland sucht aktuell freiberufliche Unterstützung als: 
&nbsp; 
Test Engineer/Verification Engineer (m/w/d) 
&nbsp; 
Aufgaben:

<ul>
	<li style="box-sizing: border-box; padding: 0px 0.7rem 0px 0px; margin: 0.5rem 0px 0.75em; display: flex; flex-direction: row; line-height: 1.5; align-items: flex-start !important;">Sie überprüfen und analysieren die Anforderungsspezifikationen auf Genauigkeit und Testbarkeit</li>
	<li style="box-sizing: border-box; padding: 0px 0.7rem 0px 0px; margin: 0.5rem 0px 0.75em; display: flex; flex-direction: row; line-height: 1.5; align-items: flex-start !important;">Sie binden die Projektbeteiligten ein und arbeiten die Ergebnisse aus</li>
	<li style="box-sizing: border-box; padding: 0px 0.7rem 0px 0px; margin: 0.5rem 0px 0.75em; display: flex; flex-direction: row; line-height: 1.5; align-items: flex-start !important;">Sie entwerfen, entwickeln oder passen Tests, Testverfahren und Testspezifikationen an&nbsp;</li>
	<li style="box-sizing: border-box; padding: 0px 0.7rem 0px 0px; margin: 0.5rem 0px 0.75em; display: flex; flex-direction: row; line-height: 1.5; align-items: flex-start !important;">Sie entwickeln und pflegen Lösungen zur Automatisierung von Tests</li>
	<li style="box-sizing: border-box; padding: 0px 0.7rem 0px 0px; margin: 0.5rem 0px 0.75em; display: flex; flex-direction: row; line-height: 1.5; align-items: flex-start !important;">Sie führen manuelle und automatisierte Tests aus</li>
	<li style="box-sizing: border-box; padding: 0px 0.7rem 0px 0px; margin: 0.5rem 0px 0.75em; display: flex; flex-direction: row; line-height: 1.5; align-items: flex-start !important;">Sie analysieren die Testergebnisse, Fehlerdokumentation und erstellen Testberichte</li>
	<li style="box-sizing: border-box; padding: 0px 0.7rem 0px 0px; margin: 0.5rem 0px 0.75em; display: flex; flex-direction: row; line-height: 1.5; align-items: flex-start !important;">Sie steuern die Kommunikation und Zusammenarbeit mit Softwareingenieuren, Qualitätsingenieuren und der Projektleitung</li>
	<li style="box-sizing: border-box; padding: 0px 0.7rem 0px 0px; margin: 0.5rem 0px 0.75em; display: flex; flex-direction: row; line-height: 1.5; align-items: flex-start !important;">Sie steuern die Aufwands- und Ressourcenschätzungen, sowie die Einhaltung von Zeitplänen</li>
</ul>

&nbsp;Qualifikation:

<ul>
	<li style="box-sizing: border-box; padding: 0px 0.7rem 0px 0px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5;">Bachelor-, Diplom- oder Masterabschluss in Elektrotechnik, Medizintechnik oder einem vergleichbaren technischem Studiengang</li>
	<li style="box-sizing: border-box; padding: 0px 0.7rem 0px 0px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5;">5 bis 10 Jahre Erfahrung in vergleichbaren Bereichen</li>
	<li style="box-sizing: border-box; padding: 0px 0.7rem 0px 0px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5;">Fähigkeit zur Einhaltung von Testplänen und -strategien in Übereinstimmung mit internen Verfahren, Standards und projektspezifischen Anforderungen</li>
	<li style="box-sizing: border-box; padding: 0px 0.7rem 0px 0px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5;">Erfahrung in der Anwendung und Bewertung angewandter Testentwurfstechniken und der Testautomatisierung</li>
	<li style="box-sizing: border-box; padding: 0px 0.7rem 0px 0px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5;">Erfahrung mit der Überprüfung von Produktanforderungen, Testentwurf, -durchführung und Änderungskontrolle</li>
	<li style="box-sizing: border-box; padding: 0px 0.7rem 0px 0px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5;">Erfahrung mit der Verbesserung des Produktdesigns und der Anforderungen im Hinblick auf die Testbarkeit</li>
	<li style="box-sizing: border-box; padding: 0px 0.7rem 0px 0px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5;">Erfahrung mit Mess- und Kontrollinstrumenten (Multimeter, Oszilloskop, Netzgerät)</li>
	<li style="box-sizing: border-box; padding: 0px 0.7rem 0px 0px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5;">Hohes Qualitäts- und Verantwortungsbewusstsein sowie hohe Zuverlässigkeit</li>
	<li style="box-sizing: border-box; padding: 0px 0.7rem 0px 0px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5;">Freude an der Arbeit an komplexen Projekten</li>
	<li style="box-sizing: border-box; padding: 0px 0.7rem 0px 0px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5;">Gute Kommunikationseigenschaften</li>
	<li style="box-sizing: border-box; padding: 0px 0.7rem 0px 0px; margin: 0.5rem 0px 0.75em; align-items: flex-start !important; display: flex; flex-direction: row; line-height: 1.5;">Gute Englischkenntnisse in Wort und Schrift</li>
</ul>

Rahmendaten: 
Start: sofort&nbsp; 
Dauer: 6 Monate 
Auslastung: 5 Tage die Woche 
Einsatzort: Baden-Württemberg

&nbsp;

&nbsp;

&nbsp;

One of our Medtech clients in Germany is currently looking for freelance support as:

&nbsp;

XXX (M/W/D) 
&nbsp; 
Tasks:

<ul>
	<li>XX</li>
</ul>

&nbsp;Qualification:

<ul>
	<li>XXX</li>
</ul>

Requirements: 
Start: XX 
Duration: XX months 
Capacity: XX days per week 
Location: XX</div>

Verification Engineer (m/w/d)

<div data-wrapper="true" style="font-size:10pt;font-family:Arial;"><div>Einer unserer Animal Health Kunden in München sucht aktuell freiberufliche Unterstützung als: 
 
Medical Manager (M/W/D) 
 
Aufgaben:
<ul>
	<li style="margin-left:8px;list-style-position:inside">Beurteilung und Beratung auf fachlicher Ebene</li>
	<li style="margin-left:8px;list-style-position:inside">Konzeption und Durchführung von Schulungen für interne und externe Kunden u. a. zu neuen Produkten</li>
	<li style="margin-left:8px;list-style-position:inside">Gestaltung und Erstellung von Broschüren</li>
	<li style="margin-left:8px;list-style-position:inside">Planung, Organisation, Implementierung, Überwachung und Analyse von klinischen Feldstudien.</li>
	<li style="margin-left:8px;list-style-position:inside">Recherche und Präsentation zu vorgegebenen Themen </li>
</ul>
 
Qualifikation:

<ul>
	<li style="margin-left:8px;list-style-position:inside">Abgeschlossenes Studium der Tiermedizin </li>
	<li style="margin-left:8px;list-style-position:inside">Erfahrungen im Kleintierbereich</li>
	<li style="margin-left:8px;list-style-position:inside">Erfahrungen im Großtierbereich sind von Vorteil</li>
	<li style="margin-left:8px;list-style-position:inside">Fundierte Marketingerfahrung sowie Erfahrung im Präsentieren vor größeren Gruppen </li>
	<li style="margin-left:8px;list-style-position:inside">Fließend Deutsch, sehr gute Englischkenntnisse </li>
</ul>
 
Rahmendaten: 
Start:asap 
Dauer: 6 Monate + 
Auslastung: 1 FTE 
Einsatzort: Remote + Onsite (Einarbeitung)</div></div>

Medical Manager

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Einer unserer Pharma-Kunden in Deutschland sucht aktuell freiberufliche Unterstützung als: 
 
Projektleiter HSE Training (M/W/D) 
 
 
Aufgaben:

<ul>
	<li style="margin-bottom:11px;list-style-position:inside">Konzeption und Etablierung eines Trainingsskonzept für den Standort der auditsicher ist</li>
	<li style="margin-bottom:11px;list-style-position:inside">Verantwortung für die Umsetzung sicherheitstechnischer und umweltrechtlicher Anforderungen in den Anlagen</li>
	<li style="margin-bottom:11px;list-style-position:inside">Beurteilung von Einrichtungen, Arbeitsmitteln, Arbeitsplätzen und Arbeitsabläufen im Einklang mit den Schutzzielen</li>
	<li style="margin-bottom:11px;list-style-position:inside">Mitarbeit bei globalen und lokalen Projekte, z.B. Recherche, Benchmark: HSE Kulturprogramm &amp; Implementierung globaler Standards</li>
	<li style="margin-bottom:11px;list-style-position:inside">Stakeholder Management</li>
</ul>

<div> 
Qualifikation:

<ul>
	<li style="margin-bottom:11px;list-style-position:inside">Naturwissenschaftlicher Background und solide Pharma-Erfahrung</li>
	<li style="margin-bottom:11px;list-style-position:inside">Berufserfahrung in HSE Projekten und tiefe Kenntnisse der HSE-Compliance-Aspekte&nbsp;</li>
	<li style="margin-bottom:11px;list-style-position:inside">Projektleitung- und Changemanagement</li>
	<li style="margin-bottom:11px;list-style-position:inside">fließende Deutsch- und Englischkenntnisse&nbsp;</li>
</ul>
</div>

 
Rahmendaten: 
Start: asap, spätestens am 01.11.2022 
Dauer: 12 Monate 
Auslastung: 1 FTE 
Einsatzort: Remote &amp; Onsite 
</div>

Projektleiter HSE Training

<div data-wrapper="true" style="font-family:Arial; font-size:10pt">
One of our Pharma clients in Switzerland&nbsp;is currently looking for support as:

European Regulatory Affairs - CTA Manager (M/W/D) 
&nbsp; 
Tasks:

<ul>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#32363a; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:left; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Provide effective operational and regulatory support for assigned regulatory submission and maintenance activities, including preparation and submission of regulatory dossiers, maintenance of regulatory databases and archives.</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#32363a; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:left; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Prepare and/or co-ordinate the preparation of regulatory documentation to support Clinical Trial Applications/amendments in the Europe (EU, UK and Switzerland). Support for rest-of-the-world clinical trial applications may be required</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#32363a; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:left; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Contribute to the regulatory strategy by bringing the European insights into discussions</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#32363a; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:left; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Interact with the cross-functional team (Regulatory, Clinical Development, Clinical Operations, Safety, CMC) to ensure optimal execution of the agreed regulatory strategy for development medicinal products</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#32363a; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:left; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Work with regulatory affairs consultants/service providers on CTA submissions</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#32363a; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:left; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Represent EU Regulatory Affairs at cross-functional study management team meetings</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#32363a; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:left; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Research relevant regulatory precedents to understand the regulatory landscape</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#32363a; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:left; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Communicate and educate cross-functional teams on European regulatory requirements and changes in the regulatory landscape</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#32363a; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:left; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Participate in process improvement initiatives as required</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#32363a; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:left; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Maintain an effective archiving and submissions/approvals tracking records</li>
</ul>

&nbsp;Qualification:

<ul>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#32363a; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:left; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Minimum of 4 years of experience managing regulatory submissions, with a primary focus on clinical trial applications and associated tasks.</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#32363a; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:left; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">BSc; MSc or PhD in a life sciences discipline.</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#32363a; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:left; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Fluent in English (written and spoken).</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#32363a; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:left; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Experience in the preparation/submission of regulatory documentation to support clinical trials applications/amendments in the European Union, Switzerland and United Kingdom. Experience with the new Clinical Trial Regulation would be an advantage.</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#32363a; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:left; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Knowledge of the European drug development process and regulatory requirements (knowledge of ex-Europe regulatory environment would be an advantage).</li>
</ul>

Requirements: 

<ul>
	<li style="list-style-position: inside;">Start: 01.12.2022</li>
	<li style="list-style-position: inside;">Duration: 30.11.2023</li>
	<li style="list-style-position: inside;">Capacity: 5 days per week</li>
	<li style="list-style-position: inside;">Location: Zug, Switzerland&nbsp;</li>
</ul>
</div>

European Regulatory Affairs - CTA Manager

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Einer unserer Pharma-Kunden in Deutschland&nbsp;sucht aktuell freiberufliche Unterstützung als: 
&nbsp; 
Experte Prozessvalidierung (M/W/D) 
&nbsp; 
Aufgaben:

<ul>
	<li>Durchführung von Prozessvalidierungen im Produktionsumfeld&nbsp;&nbsp;</li>
	<li>Risikoanalysen</li>
	<li>Requalifizierung von Anlagen &amp; Räumen</li>
	<li>Erstellung von Reinraumkonzepten&nbsp;</li>
</ul>

&nbsp;Qualifikation:

<ul>
	<li>Langjährige Erfahrung im Bereich Prozessvalidierung</li>
	<li>Expertise in der Requalifizierung von Anlagen &amp; Räumen</li>
	<li>Profunde Kenntnisse des pharmazeutisch-regulierten Umfelds (GMP)</li>
	<li>Sehr gute Deutsch- und Englischkenntnisse</li>
</ul>

Rahmendaten: 
Start: Ab sofort spät. 01.11 
Dauer: 6 Monate 
Auslastung: 4 Tage die Woche 
Einsatzort: Vor Ort &amp; remote

&nbsp;

&nbsp;
</div>

Experte Prozessvalidierung (M/W/D)

<div data-wrapper="true" style="font-size:10pt;font-family:Arial;">Einer unserer Medizintechnik-Kunden in Deutschland sucht aktuell freiberufliche Unterstützung als: 
&nbsp; 
Experte Spektroskopie &amp; Fluoreszenz (M/W/D) 
&nbsp; 
Aufgaben:

<ul>
	<li>Beratung bei der Entwicklung &amp; Bewertung verschiedener Verfahren&nbsp;</li>
	<li>Internes &amp; externes Stakeholder Management</li>
	<li>Entwicklung von Indikationen &amp; Workflows</li>
	<li>Beratung aus biologischer/medizinscher Sicht in Bezug auf optische Systeme der Spektralanalytik</li>
</ul>

&nbsp;Qualifikation:

<ul>
	<li>Studium der Physik, Ingenieurswissenschaften, Naturwissenschaften, Medizin oder vergleichbarer Abschluss</li>
	<li>Erfahrung mit Spektroskopie und Fluoreszenz</li>
	<li>Nice to have: Erfahrung mit bildgebenden Verfahren</li>
	<li>Sprachen: Deutsch &amp; Englisch</li>
</ul>

Rahmendaten: 
Start: ab sofort 
Dauer: 6+ Monate&nbsp; 
Auslastung: 3-5 Tage/Woche, davon mind. 2 Tage vor Ort</div>

Experte Spektroskopie & Fluoreszenz

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
One of our Clients in Germany is currently looking for freelance support as: 
&nbsp; 
IT System Engineer - Storage/Backup/Recovery (M/W/D). 
&nbsp; 
Tasks:

<ul>
	<li style="list-style-position: inside;">Operation of a new backup solution</li>
	<li style="list-style-position: inside;">Migration of the former backup solution</li>
	<li style="list-style-position: inside;">System checks</li>
	<li style="list-style-position: inside;">Testing of the backups</li>
	<li style="list-style-position: inside;">Support</li>
	<li style="list-style-position: inside;">Change-Management</li>
	<li style="list-style-position: inside;">Communication with producer support</li>
	<li style="list-style-position: inside;">Technical support of the tape library and import of backup tapes</li>
	<li style="list-style-position: inside;">Monitoring the transfer via Amazon Web Services to the cloud</li>
</ul>

<div>&nbsp;Qualifications:</div>

<div>&nbsp;</div>

<ul>
	<li style="list-style-position: inside;">Extensive experience with the following tools, Commvault, Cohesity and NetApp</li>
	<li style="list-style-position: inside;">Experience with cloud technologies especially the AWS Cloud</li>
	<li style="list-style-position: inside;">Know-how in dealing with system migrations</li>
	<li style="list-style-position: inside;">Fluent in english, german optional</li>
</ul>

<div>Requirements:</div>

<ul>
	<li style="list-style-position: inside;">Start: immediately</li>
	<li style="list-style-position: inside;">Duration: 6 months</li>
	<li style="list-style-position: inside;">Workload: 25 hours per week</li>
	<li style="list-style-position: inside;">Location: remote</li>
</ul>

<div>&nbsp;</div>
</div>

IT System Engineer - Storage/Backup/Recovery (m/w/d)

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
<table cellspacing="0" class="Table" style="border-collapse:collapse">
	<tbody>
		<tr>
			<td style="border-bottom:1px solid #a3a3a3; border-left:1px solid #a3a3a3; border-right:1px solid #a3a3a3; border-top:1px solid #a3a3a3; padding:5px 5px 5px 5px; vertical-align:top; width:634px">Einer unserer&nbsp;Pharma-Kunden in Deutschland&nbsp;sucht aktuell freiberufliche Unterstützung als: 
			&nbsp; 
			Insights and Analytics Manager (M/W/D) 
			&nbsp; 
			Aufgaben:
			<ul>
				<li class="x" style="list-style-position:inside">Unterstützende Beratung zur Optimierung der Prozesse</li>
				<li class="x" style="list-style-position:inside">Konzeption, Steuerung und Analyse von qualitativen und quantitativen Ad-hoc-Primärmarktforschungsprojekten</li>
				<li style="list-style-position:inside">Suche und Bewertung neuer und relevanter Marktforschungsmethoden</li>
				<li class="x" style="list-style-position:inside">Analyse von Sekundärmarktdaten und Entwicklung von Patientenmodellen</li>
				<li class="x" style="list-style-position:inside">Beratender Ansprechpartner für die internen Kollegen</li>
				<li class="x" style="list-style-position:inside">Dokumentation und Datenmanagement</li>
				<li class="x" style="list-style-position:inside">Abstimmung mit den lokalen Stakeholdern</li>
				<li class="x" style="list-style-position:inside">Multichannel Management </li>
			</ul>
			 
			Qualifikation:

			<ul>
				<li style="list-style-position:inside">fundierte Erfahrung in der Marktforschung, vorzugsweise in der pharmazeutischen Industrie</li>
				<li class="x" style="list-style-position:inside">CRM-Erfahrung im Salesforce Umfeld als idealerweise als User</li>
				<li class="x" style="list-style-position:inside">Must have: Erfahrung mit Veeva &amp; Foundry </li>
				<li class="x" style="list-style-position:inside">Must have: Deutsch &amp; English</li>
			</ul>
			&nbsp; 
			Rahmendaten: 
			Start: ab sofort 
			Dauer: 5 Monate 
			Auslastung: 4-5 Tage die Woche 
			Einsatzort: remote </td>
		</tr>
	</tbody>
</table>
</div>

Sales Force Effectiveness Manager

<div data-wrapper="true" style="font-size:10pt;font-family:Arial;">One of our Pharma clients in Germany is currently looking for freelance support as:

&nbsp;

Statistical Programmer (M/W/D) 
&nbsp; 
Tasks:

<ul>
	<li style="box-sizing: border-box;">Responsible for all the relevant programming activities (including but not limited to SDTM, ADAM and TFLs).</li>
	<li style="box-sizing: border-box;">Statistical programming to regulatory and market access submission and know-how transfer in quick turnaround in response to regulatory agencies.</li>
	<li style="box-sizing: border-box;">Detect errors in detail and correct. e.g., review tables/listings, edit checks output and SAS programs to ensure quality of deliverables.</li>
	<li style="box-sizing: border-box;">Development of programming documentation including, but not limited to, specifications.</li>
	<li style="box-sizing: border-box;">In-depth knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.</li>
	<li style="box-sizing: border-box;">Design and maintenance of statistical datasets for multiple stakeholder groups.</li>
</ul>

&nbsp;Qualification:

<ul>
	<li style="box-sizing: border-box;">Project experience 8-11 years in programming Pharmaceutical Industries</li>
	<li style="box-sizing: border-box;">University degree from an accredited institution in a technical field such as computer science or mathematics; Master’s degree in bio/statistics preferred.</li>
	<li style="box-sizing: border-box;">Fluent written and spoken English is required</li>
	<li style="box-sizing: border-box;">Knowlegde in use of SAS is necessary</li>
	<li style="box-sizing: border-box;">Nice to have project experience in Cardiovascular and Oncology areas</li>
</ul>

Requirements: 
Start: 04.10.2022 
Duration: until 28.03.2023 
Capacity: 5 days per week 
Location: 100% remote</div>

Consultant Statistical Programmer (m/w/d)

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Einer unserer Pharmakunden in Schleswig-Holstein&nbsp;sucht aktuell freiberufliche Unterstützung als: 
&nbsp; 
Interim Head of Treasury (M/W/D) 
&nbsp; 
Aufgaben:

<ul>
	<li>Vorbereitung, Durchführung und Verwaltung von Finanzierungen</li>
	<li>Ausbau und Weiterentwicklung geeigneter Finanzierungsstrukturen</li>
	<li>Beratung im Liquiditätsmanagement sowie Fördermittelexpertise</li>
	<li>Beratung im Bereich Investitionen</li>
	<li>Bonitätsüberwachung, Währungs- und Zinsmanagement</li>
</ul>

&nbsp;Qualifikation:

<ul>
	<li>Abgeschlossenes betriebswirtschaftliches Studium mit Schwerpunkt Finanzen</li>
	<li>Mind. 5 Jahre Erfahrung in einem vergleichbaren Aufgabengebiet</li>
	<li>Große Expertise in Finanzierungsfragen</li>
	<li>Must-have: fließende Englisch-Kenntnisse</li>
</ul>

Rahmendaten: 
Start: Oktober 
Dauer: 10-12 Monate 
Auslastung: 4-5 Tage pro Woche 
Einsatzort: remote+onsite

&nbsp;

&nbsp;

&nbsp;
</div>

Interim Head of Treasury

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Einer unserer Pharmakunden in Schleswig-Holstein&nbsp;sucht aktuell freiberufliche Unterstützung als: 
&nbsp; 
Medical Manager / Onkologie (M/W/D) 
&nbsp; 
Aufgaben:

<ul>
	<li>Begleitung des deutschen Launches eines neuen Onkologie-Produkts</li>
	<li>Mitarbeit an medizinisch-wissenschaftlichen Strategien zur Positionierung</li>
	<li>Begleitung und aktive Mitarbeit von AMNOG-Prozessen</li>
	<li>Aufbau, Etablierung und Pflege von KOL-Netzwerk</li>
	<li>Erarbeitung, Organisation und Durchführung von Produkt- und Indikationsschulungen</li>
	<li>Beantwortung medizinischer Anfragen</li>
</ul>

&nbsp;Qualifikation:

<ul>
	<li>Abgeschlossenes Studium der Naturwissenschaften, Medizin oder Pharmazie, Promotion wünschenswert</li>
	<li>Launch-Erfahrung in Deutschland</li>
	<li>Erfahrung mit AMNOG-Prozessen</li>
	<li>Fundiertes Wissen im Bereich Onkologie/Mammakarzinom</li>
	<li>Must Have: Netzwerk von deutschen KOLs im Bereich Onkologie</li>
	<li>Deutsch- und Englisch-Kenntnisse</li>
</ul>

Rahmendaten: 
Start: Oktober / spät. Dezember&nbsp; 
Dauer: 12 Monate 
Auslastung: 20-40 Stunden pro Woche 
Einsatzort: remote + onsite&nbsp;

&nbsp;

&nbsp;
</div>

Medical Manager / Onkologie

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Einer unserer Medizintechnik-Kunden in Deutschland sucht aktuell freiberufliche Unterstützung als: 
&nbsp; 
Lifecycle Projektleiter (M/W/D) 
&nbsp; 
Aufgaben:

<ul>
	<li class="paragraph" style="list-style-position:inside;">Koordination, Abstimmung und Überwachung der Maßnahmen- und Ressourcenplanung und Maßnahmenumsetzung der verschiedenen Lifecycle-Projekte </li>
	<li class="paragraph" style="list-style-position:inside;">Pflege der Ticket-Übersicht (Abwicklung, Bündelung, Bewertung, Koordination)&nbsp; </li>
	<li class="paragraph" style="list-style-position:inside;">Interdisziplinäre Zusammenarbeit mit Lifecycle-Team, Moderation der Meetings </li>
	<li class="paragraph" style="list-style-position:inside;">Unterstützung der Pflege der Produktdokumentation</li>
</ul>

&nbsp;Qualifikation:

<ul>
	<li class="paragraph" style="list-style-position:inside">Studium im Bereich Ingenieurswissenschaft, Physik oder einer vergleichbar</li>
	<li class="paragraph" style="list-style-position:inside">Erfahrung in der Leitung von Entwicklungsprojekten&nbsp;</li>
	<li class="paragraph" style="list-style-position:inside">Erfahrung in der Entwicklung sicherheitskritischer medizintechnischer Systeme, idealerweise im Lifecycle-Management medizinischer Geräte&nbsp;</li>
	<li class="paragraph" style="list-style-position:inside">Kenntnisse ISO 13485, 60601</li>
	<li class="paragraph" style="list-style-position:inside">Deutsch fließend</li>
	<li class="paragraph" style="list-style-position:inside">Kommunikationsstärke, sehr gute Projektmanagementkenntnisse</li>
</ul>

Rahmendaten: 
Start: ab sofort, spätestens 17.10.22 
Dauer: 6 Monate + 
Auslastung: 4-5 Tage die Woche 
Einsatzort: Thüringen &amp; Remote (nach Einarbeitung flexibel)
</div>

Lifecycle Projektleiter

<div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Einer unserer Medizintechnik-Kunden in Deutschland sucht aktuell freiberufliche Unterstützung als: 
&nbsp; 
Quality Spezialist Biologische Sicherheit (M/W/D) 
&nbsp; 
Aufgaben:

<ul>
	<li><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#212529; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:left; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Definition, Umsetzung &amp; Nachweis sowie die Überwachung der biologischen und chemischen Sterilitätsanforderungen</li>
	<li><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; color:#212529; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:left; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Bewertung der Produkte und Prozesse hinsichtlich Biokompatibilität, Sterilisierbarkeit und biologische Sicherheit</li>
	<li>Testplanüberwachung &amp; Aufbereitung der Testergebnisse</li>
</ul>

&nbsp;Qualifikation:

<ul>
	<li>Naturwissenschaftliches Studium oder vergleichbarer Abschluss</li>
	<li>Erfahrung im Bereich biologische Sicherheit für Medizinprodukte Klasse II</li>
	<li>Erfahrung mit EO Sterilisation</li>
	<li>Normenverständnis: MDR, ISO 13485 / 11737 / 11135 / 11137 / 11607 / 10993</li>
</ul>

Rahmendaten: 
Start: Ab sofort 
Dauer: mind. 3 Monate 
Auslastung: 4-5 Tage die Woche (80% vor Ort) 
Einsatzort: Thüringen

&nbsp;

&nbsp;
</div>

Quality Spezialist Biologische Sicherheit

<div data-wrapper="true" style="font-size:10pt;font-family:Arial;"><div>Clinical Site Manager (M/F/*) 
&nbsp; 
Special emphasis lies on: 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Experience with study-start-up activities 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Patient Recruitment 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Site oversight and proactive/forward-looking issue management 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Capability to liaison with CRAs, KOLs, PIs (relationship management) 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Document &amp; track monitoring 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Support site audit preparations 
&nbsp; 
Qualifications&nbsp;: 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Extensive experience with site management &amp; oversight, monitoring processes 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Being able to act as trouble-shooter and create high-performance environment 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; History of ensuring GCP adherence and applying risk management 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Experience with highly complex studies 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 5+ years of PM and 3+ years of monitoring 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Very good communication &amp; organizational skills 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Business fluency in Turkish &amp; English 
&nbsp; 
Requirements: 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Start: asap, there is some flexibility 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; FTE: full-time would be ideal 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Duration: 6 – 12 months 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Location: remote + travel as far as possible within Turkey, most sites are in Istanbul 
&nbsp;</div></div>

Clinical Site Manager // Study Project Manager

<div data-wrapper="true" style="font-size:10pt;font-family:Arial;"><div>Senior Social Media Listening Lead - EEMEA (M/F/*) 
&nbsp; 
Tasks:
<ul>
	<li style="margin-left:8px;list-style-position:inside">Focus on Engaging in the ESMG’s social media ecosystem</li>
	<li style="margin-left:8px;list-style-position:inside">Partner with local teams – digital and franchise teams - to support selected priority in-market Social Media Marketing activities, provide needed counsel on social media marketing strategies, and support the development of the social media marketing framework program</li>
	<li style="margin-left:8px;list-style-position:inside">Partnering with Digital teams and franchise teams to provide Social Media Marketing expertise and recommendations that are beneficial to local teams with an integrated approach</li>
	<li style="margin-left:8px;list-style-position:inside">Lead Engagement efforts that includes:
	<ul style="list-style-type:circle">
		<li style="margin-left:8px; list-style-position:inside">Advancing Social Media Marketing Capabilities</li>
		<li style="margin-left:8px; list-style-position:inside">Paid Media</li>
		<li style="margin-left:8px; list-style-position:inside">Influencer Management</li>
	</ul>
	</li>
	<li style="margin-left:8px;list-style-position:inside">Work with EEMEA Social Media Listening Lead to collectively track operations including metrics across key capabilities of Listen, Publish and Engage.</li>
	<li style="margin-left:8px;list-style-position:inside">Under the guidance of EEMEA Digital Engagement Lead to partner closely with ESMG team and the global agency in EEMEA to align work and stakeholders</li>
	<li style="margin-left:8px;list-style-position:inside">Support the utilization of global tools for efficiency such as Salesforce Social Studio, Kapost</li>
	<li style="margin-left:8px;list-style-position:inside">Guide local teams on Engage related compliance (policies, SOPs, processes)</li>
</ul>
&nbsp; 
Qualifications:

<ul>
	<li style="margin-left:8px;list-style-position:inside">Bachelor’s degree required</li>
	<li style="margin-left:8px;list-style-position:inside">At least 8 years of working experience in marketing, communications, social media/social media marketing, or digital</li>
	<li style="margin-left:8px;list-style-position:inside">Experienced with health care industry (pharmaceutical as a focus) is a plus</li>
	<li style="margin-left:8px;list-style-position:inside">Project management experience: strategic planning, operation and execution</li>
	<li style="margin-left:8px;list-style-position:inside">Social media and digital marketing experience – have personally plan and/or execute several successful campaigns in the last 3 years</li>
	<li style="margin-left:8px;list-style-position:inside">Strong digital/social media marketing background</li>
	<li style="margin-left:8px;list-style-position:inside">Marketing experience across target audiences (HCPs, Patients/Consumers, Public) would be an asset</li>
	<li style="margin-left:8px;list-style-position:inside">Planning/operational/executional experience moving teams and projects to completion and achieve objectives</li>
	<li style="margin-left:8px;list-style-position:inside">Leading meetings and engaging multiple stakeholders to understand objectives, business or communications needs and priorities</li>
	<li style="margin-left:8px;list-style-position:inside">Ability to function successfully on strategy and implementation</li>
	<li style="margin-left:8px;list-style-position:inside">Ability to apply data to insights</li>
	<li style="margin-left:8px;list-style-position:inside">Ability to work in a fast-paced environment and with cross-functional teams</li>
	<li style="margin-left:8px;list-style-position:inside">Above-market regional team experience and success of partnering with in-market teams</li>
	<li style="margin-left:8px;list-style-position:inside">Ability to deliver and thrive under pressure and tight timelines</li>
	<li style="list-style-position:inside">Proven communication and strong organizational skills</li>
	<li style="list-style-position:inside">Languages: English (business fluent)</li>
</ul>
&nbsp; 
Frame Data:

<ul>
	<li style="list-style-position:inside">Start: Asap</li>
	<li style="list-style-position:inside">Duration: 12 months</li>
	<li style="list-style-position:inside">Capacity: Full-time onsite + remote</li>
	<li style="list-style-position:inside">Location: Lucerne, Switzerland</li>
</ul>
</div></div>

Senior Social Media Listening Lead - EEMEA

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
One of our Biotech/Medical Device clients in Germany is currently looking for freelance support as:

&nbsp;

Sales Agent Germany Surgery (D/M/W) 
&nbsp; 
Tasks:

<ul>
	<li>Actively and enthusiastically develop the German market</li>
	<li>Achievement of sales objectives</li>
	<li>Support active and potential customers on a product and procedural/administrative level</li>
	<li>Identify growth opportunities</li>
	<li>Continuous reporting and evaluation of results</li>
</ul>

&nbsp;

&nbsp;Qualification:

<ul>
	<li>Bachelor's Degree with 5+ years sales experience in medical sales</li>
	<li>High affinity / enthusiasm to market highly scientific and technologically advanced medical products</li>
	<li>Ability of eye-to-eye conversations with surgeons (hand, trauma, orthopedics) sales experience</li>
	<li>Good understanding of Operating Rooms and surgeons’ working environment</li>
	<li>Ability to understand and use complex clinical studies as a sales tool</li>
	<li>German and English business fluency</li>
	<li>Willingness to travel as required</li>
	<li>Understanding of the German NUB Verfahren is an asset</li>
</ul>

&nbsp;

Requirements: 
Start: beginning of January 2023 
Duration: 6 months+ 
Capacity: from 20 hours / week 
Residency in Bavaria or Baden-Wuerttemberg (possibly North/East Germany)
</div>

Sales Agent Surgery (D/M/W)

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
<div>Social Media Listening Lead - EEMEA (M/F/*) 
&nbsp; 
Tasks:
<ul>
	<li style="list-style-position:inside">Relationship management – to work with various internal and external stakeholders ie. Account leads, clients, creative team, finance team</li>
	<li style="list-style-position:inside">Social Listening – to stay abreast of conversations online about the client/brand, product or campaign. To monitor content performance of campaigns.</li>
	<li style="list-style-position:inside">Social/Network Analysis – to scrutinize social structures and establish meaning of the relationships or interactions between users</li>
	<li style="list-style-position:inside">Problem Analysis – to identify problem areas, and optimize or propose solutions with the insights gained from social listening and data reports</li>
	<li style="list-style-position:inside">KPI Development – Develop and implement strategic measurement plans to ensure accurate measure of Key Performance Indications (KPIs)</li>
	<li style="list-style-position:inside">Report Presentation – to systematically translate complex analysis into concise statistics to support the insights for clients. To collate and do campaign reporting using digital/web analytics</li>
	<li style="list-style-position:inside">Social media – be an expert in social platforms such as Facebook, Instagram, Twitter, Linkedin etc and to buy social ads in the planning or execution phases</li>
</ul>
&nbsp; 
Qualifications:

<ul>
	<li style="list-style-position:inside">Should have 4-5 years of relevant experience, preferably in a media or an agency environment </li>
	<li style="list-style-position:inside">Understand and be able to construct Boolean search queries</li>
	<li style="list-style-position:inside">Demonstrate strong understanding of social listening platforms </li>
	<li style="list-style-position:inside">Demonstrated ability to understand business goals and develop unique media opportunities that deliver on the business goal. </li>
	<li style="list-style-position:inside">Solid quantitative/analytical skills and strong attention to detail</li>
	<li style="list-style-position:inside">Proven track record of conceptualizing programs, selling-in internally and executing</li>
	<li style="list-style-position:inside">Ability to interface and manage cross functional internal and client teams</li>
	<li style="list-style-position:inside">Experience interacting with vendors/contractors, including effective project scoping, managing for results, and financial and operational accountability</li>
	<li style="list-style-position:inside">Have excellent written and verbal communication skills; comfortable delivering recommendations to all management levels</li>
	<li style="list-style-position:inside">Think critically and creatively, meaning the ability to think clearly and rationally, solve problems and develop new and useful possibilities</li>
	<li style="list-style-position:inside">Languages: English (business fluent)</li>
</ul>
&nbsp; 
Frame Data:

<ul>
	<li style="list-style-position:inside">Start: Asap</li>
	<li style="list-style-position:inside">Duration: 12 months</li>
	<li style="list-style-position:inside">Capacity: Full-time onsite + remote</li>
	<li style="list-style-position:inside">Location: Lucerne, Switzerland</li>
</ul>
</div>
</div>

Social Media Listening Lead -EEMEA

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
<div>Manager Medical Research Operations (M/F/*) 
&nbsp; 
The Manager, MRO provides operational expertise in and oversight of the execution of post-drug approval research. The role is part of the Worldwide Medical Operations &amp; Effectiveness function within Worldwide Medical Affairs. The work is collaborative and is performed in conjunction with medical teams in both the global headquarters and at local affiliates. 
&nbsp; 
The successful candidate will act as an operational partner in driving data generation program execution. Working across late-stage development and marketed products, the incumbent will manage the operations for Phase 4 studies, patient registries, outcomes research, and real-world evidence programs. Activities include study planning, start-up, vendor management, site management, tracking and reporting. 
&nbsp; 
Tasks:
<ul style="unicode-bidi:embed" type="disc">
	<li style="vertical-align:middle">Support all project management activities for data generation projects as assigned&nbsp;</li>
	<li lang="en-US" style="vertical-align:middle">Operationalize data generation projects in close collaboration with the Program Lead: Review committee coordination, contracting, study management team formation, publication support, filing, milestones and budget</li>
	<li lang="en-US" style="vertical-align:middle">Provide regular updates to internal clinical trial management system for departmental projects, and compile reports from the system </li>
	<li lang="en-US" style="vertical-align:middle">Support the Associate Director Medical Research Operations Study Management with tracking and update of the medical dashboard </li>
	<li lang="en-US" style="vertical-align:middle">Act as a key point of contact between Medical Research Operations group and the external research stakeholders and partners</li>
</ul>
&nbsp; 
Qualifications:

<ul style="unicode-bidi:embed" type="disc">
	<li lang="en-US" style="vertical-align:middle">Minimum of 7+ years of clinical research experience with minimum of 5+ years of CRO/Sponsor Project Management</li>
	<li lang="en-US" style="vertical-align:middle">Strong Project Management skills including risk assessment and contingency planning</li>
	<li lang="en-US" style="vertical-align:middle">Demonstrated learning agility</li>
	<li lang="en-US" style="vertical-align:middle">Possess a combination of critical thinking and operational know-how and efficiency</li>
	<li lang="en-US" style="vertical-align:middle">Demonstrated success in working independently</li>
	<li lang="en-US" style="vertical-align:middle">High level of customer orientation, awareness and focus</li>
	<li lang="en-US" style="vertical-align:middle">Strong team leadership skills</li>
	<li lang="en-US" style="vertical-align:middle">Preference for experience with late phase, post-market, and observational clinical research</li>
	<li lang="en-US" style="vertical-align:middle">Neuroscience or rare disease experience preferred </li>
	<li lang="en-US" style="vertical-align:middle">Exceptional analytical, problem-solving, and troubleshooting abilities.</li>
	<li lang="en-US" style="vertical-align:middle">Strong written and verbal communication skills.</li>
	<li style="vertical-align:middle">Languages: English (business fluent)</li>
</ul>
&nbsp; 
Frame Data:

<ul style="unicode-bidi:embed" type="disc">
	<li style="vertical-align:middle">Start: Asap</li>
	<li style="vertical-align:middle">Duration: 8 months</li>
	<li style="vertical-align:middle">Capacity: Full-time</li>
	<li style="vertical-align:middle">Location: Baar, Switzerland</li>
</ul>
</div>
</div>

Manager Medical Research Operations

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
<div>One of our pharmaceutical clients in Germany is currently seeking freelance support as: 
 
CQV Engineers (M/W/D) 
 
 
 
Qualification:
<ul>
	<li style="-webkit-font-smoothing: antialiased; box-sizing: border-box; font-style: inherit; font-weight: inherit; margin-left: 25px;">Ideally qualified Chemical/Mechanical/Biochemical/Biopharma Engineer, but this is not mandatory.</li>
	<li style="-webkit-font-smoothing: antialiased; box-sizing: border-box; font-style: inherit; font-weight: inherit; margin-left: 25px;">Minimum 3-5 year experience working as&nbsp;C&amp;Q engineer</li>
	<li style="-webkit-font-smoothing: antialiased; box-sizing: border-box; font-style: inherit; font-weight: inherit; margin-left: 25px;">Experience in field commissioning of black Utilities /clean Utilities&nbsp;/ process Equipment&nbsp;USP&nbsp;(e.g. bioreactors, Media Prep, Media Hold, Harvest),&nbsp;DSP&nbsp;(e.g. Buffer Prep, Buffer Hold, Chroma Skids, Process Stations) auxillaries (Autoclaves / part washers, clean benches, etc.)</li>
	<li style="-webkit-font-smoothing: antialiased; box-sizing: border-box; font-style: inherit; font-weight: inherit; margin-left: 25px;">Preferred experience in commissioning using&nbsp;Siemens PCS7&nbsp;or similar&nbsp;automation&nbsp;packages.</li>
	<li style="-webkit-font-smoothing: antialiased; box-sizing: border-box; font-style: inherit; font-weight: inherit; margin-left: 25px;">Preferred experience working on 2 or more&nbsp;Biopharmaceutical/Biotech/Pharmaceutical&nbsp;Projects (no packaging projects)</li>
	<li style="-webkit-font-smoothing: antialiased; box-sizing: border-box; font-style: inherit; font-weight: inherit; margin-left: 25px;">Experience problem solving; Team players; Field knowledge, hands-on approach ( no managerial function) mandatory</li>
	<li style="-webkit-font-smoothing: antialiased; box-sizing: border-box; font-style: inherit; font-weight: inherit; margin-left: 25px;">Experience in mentoring team members</li>
	<li style="-webkit-font-smoothing: antialiased; box-sizing: border-box; font-style: inherit; font-weight: inherit; margin-left: 25px;">Energetic, positive, and proactive</li>
	<li style="-webkit-font-smoothing: antialiased; box-sizing: border-box; font-style: inherit; font-weight: inherit; margin-left: 25px;">Not averse to work in a 6 day week scenario</li>
	<li style="-webkit-font-smoothing: antialiased; box-sizing: border-box; font-style: inherit; font-weight: inherit; margin-left: 25px;">English language mandatory, also German could be an advantage</li>
</ul>
 
Key data: 

<ul>
	<li style="-webkit-font-smoothing: antialiased; box-sizing: border-box; font-style: inherit; font-weight: inherit; margin-left: 25px;">Start: May / June 2022</li>
	<li style="-webkit-font-smoothing: antialiased; box-sizing: border-box; font-style: inherit; font-weight: inherit; margin-left: 25px;">FTE: ideally full-time on site</li>
	<li style="-webkit-font-smoothing: antialiased; box-sizing: border-box; font-style: inherit; font-weight: inherit; margin-left: 25px;">Duration: 6-10 months</li>
	<li style="-webkit-font-smoothing: antialiased; box-sizing: border-box; font-style: inherit; font-weight: inherit; margin-left: 25px;">Conditions: Daily Rate (+-9h)&nbsp;</li>
	<li style="-webkit-font-smoothing: antialiased; box-sizing: border-box; font-style: inherit; font-weight: inherit; margin-left: 25px;">Location: South of Germany</li>
</ul>
</div>
</div>

CQV Experts

<div data-wrapper="true" style="font-size:10pt;font-family:Arial;">Einer unserer Medizintechnik-Kunden in der Schweiz&nbsp;sucht aktuell freiberufliche Unterstützung als: 
&nbsp; 
Inbetriebnehmer (M/W/D) 
&nbsp; 
Aufgaben:

<ul>
	<li>Optimierung der Montageanlagen</li>
	<li>Arbeitsanweisungen ergänzen/erweitern</li>
	<li>Wartungsanweisungen ergänzen/anpassen</li>
	<li>Beheben von komplexen Anlagenstörungen</li>
	<li>Anpassung der Qualifizierungsdokumente auf die spezifischen neuen Anlagen</li>
	<li>Qualifizierung der Anlagen (Testpläne schreiben im Abgleich mit den Lastenheften, Testreihen fahren und dokumentieren)</li>
	<li>Ggfs. Validierung der Prozesse</li>
</ul>

&nbsp;Qualifikation:

<ul>
	<li>Erfahrung im Anlagenbau und dessen Bedienung</li>
	<li>Kenntnisse im Bereich Automatisierung/Maschinenbau</li>
	<li>Qualifizierungserfahrung von Anlagen wünschenswert</li>
	<li>Hands on</li>
	<li>Deutschkenntnisse</li>
</ul>

Rahmendaten: 
Start: asap 
Dauer: 6 Monate 
Auslastung: 5 Tage die Woche 
Einsatzort: Solothurn</div>

Inbetriebnehmer

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Einer unserer Kunden in Deutschland sucht aktuell freiberufliche Unterstützung als: 
&nbsp; 
Oracle Datenbank Entwickler (M/W/D) 
&nbsp; 
Aufgaben:

<div>
<ul>
	<li style="margin-top: 19px; margin-left: 45px; list-style-position: inside;">Analyse der datenbankbasierten Software­ </li>
	<li style="margin-left: 45px; list-style-position: inside;">Entwickeln der Prozesse zur Instandhaltung und Testen der Oracle-Datenbank </li>
	<li style="margin-left: 45px; list-style-position: inside;">Überprüfen des Leistungs­verhaltens durch ständige Analyse und Optimierung </li>
	<li style="margin-left: 45px; list-style-position: inside;">Fehleranalysen und -behebungen </li>
	<li style="margin-bottom: 19px; margin-left: 45px; list-style-position: inside;">Erstellen von Projekt­dokumentationen </li>
</ul>
</div>

&nbsp;Qualifikation:

<ul>
	<li style="margin-top: 19px; margin-left: 45px; list-style-position: inside;">Erfahrungen in der Oracle Datenbankentwicklung&nbsp;</li>
	<li style="margin-left: 45px; list-style-position: inside;">Erweiterte Kenntnisse mit Identity Management Systemen, speziell Oracle Waveset&nbsp;</li>
	<li style="margin-left: 45px; list-style-position: inside;">Java-Kenntnisse </li>
	<li style="margin-bottom: 19px; margin-left: 45px; list-style-position: inside;">Gute Deutsch und Englischkenntnisse </li>
</ul>

Rahmendaten: 
Start: ab sofort - spätestens 01.10.22 
Dauer: 4 Monate 
Auslastung: 3-5 Tage die Woche 
Einsatzort: Remote
</div>

Oracle Datenbank Entwickler (m/w/d)

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-size:10pt;font-family:Arial;">Einer unserer Pharma-Kunden in Deutschland sucht aktuell freiberufliche Unterstützung als: 
&nbsp; 
Projekteiter CRM (M/W/D) 
&nbsp; 
Aufgaben:

<ul>
	<li style="box-sizing: border-box;">Leitung des agilen Prozesses der Einführung und der Optimierung der CRM&nbsp; Landschaft</li>
	<li style="box-sizing: border-box;">Ownership für das CRM-System hinsichtlich der aller Fragestellungen inkl. Infrastruktur, Architektur, Daten und Tools</li>
	<li style="box-sizing: border-box;">Optimierung des CRM-Systems und Integration von Marketing und Vertriebsprozessen&nbsp;</li>
	<li style="box-sizing: border-box;">Betreuung von Sales und Marketing zu CRM-Fragen in&nbsp;Kooperation mit&nbsp; IT</li>
	<li style="box-sizing: border-box;">Definition einer CRM-Roadmap im Einklang mit der Unternehmensstrategie</li>
	<li style="box-sizing: border-box;">Priorisierung der Use Cases entsprechend der Unternehmensziele&nbsp; sowie&nbsp;Projekt Controlling</li>
	<li style="box-sizing: border-box;">Vorbereitung und Durchführung von Schulungen und Workshops</li>
</ul>

&nbsp;Qualifikation:

<ul>
	<li style="box-sizing: border-box;">Berufserfahrung in den Bereichen, Sales, Marketing, IT und in einer CRM-lastigen Position</li>
	<li style="box-sizing: border-box;">Gute Kenntnisse in JIRA, Azure DevOps (oder vergleichbarer Tools), MS-Office/Google Workspace und SCRUM&nbsp;</li>
	<li style="box-sizing: border-box;">Hohes Verständnis von Sales- &amp; Marketing-Prozessen&nbsp;</li>
	<li style="box-sizing: border-box;">Track Record im Projektmanagement, agilen Projektmethoden und Lean Startup in der Produktentwicklung</li>
	<li style="box-sizing: border-box;">Gute Kenntnisse&nbsp; in der Leitung von agilen Projekten&nbsp;</li>
	<li style="box-sizing: border-box;">Erfahrung im Pharmabereich wünschenswert</li>
	<li style="box-sizing: border-box;">Kenntnisse in Salesforce, VEEVA, MS Dynamics sind von Vorteil</li>
	<li style="box-sizing: border-box;">Zertifizierung als Professional Scrum Product Owner (PSPO I) oder Professional Scrum Master (PSM I) ist wünschenswert</li>
	<li style="box-sizing: border-box;"> 
	Start: asap, spätetstens zum 15.10.2022 
	Dauer: 6 Monate 
	Auslastung: 4-5 Tage die Woche 
	Einsatzort: Remote, gelegentlich Onsite</li>
</ul>

&nbsp;</div>

Product Owner CRM (m/w/d)

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Einer unserer Pharma-Kunden in Deutschland sucht aktuell freiberufliche Unterstützung als: 
&nbsp; 
Digital Marketing Manager/Digital Native (M/W/D) 
&nbsp; 
Aufgaben:

<ul>
	<li style="box-sizing: border-box;">Strategische Planung, Umsetzung und Optimierung von Performance Kampagnen</li>
	<li style="box-sizing: border-box;">Mitgestaltung der eCommerce-Strategie in Zusammenarbeit mit externen Partnern&nbsp;</li>
	<li style="box-sizing: border-box;">Steuerung von Social Media Kampagnen(Facebook/Instagram)</li>
	<li style="box-sizing: border-box;">Nutzung von Online-Tools wie Google Ads Editor oder Amazon Seller Central und Beherrschung von Digital Analytics-Themen</li>
	<li style="box-sizing: border-box;">KPI-Überwachung und Erstellung von Reportings via Power BI.</li>
	<li style="box-sizing: border-box;">Konzeption und Umsetzung von Digital Marketing Kampagnen wie Tracking, Influencer-Marketing oder den Aufbau eines TikToK-Accounts.</li>
</ul>

&nbsp;Qualifikation:

<ul>
	<li style="box-sizing: border-box;">Mehrjährige Berufserfahrung im Bereich SEA, Paid Social Ads und Amazon PPC.</li>
	<li style="box-sizing: border-box;">Gute Kenntnisse in Web Design und vorhandene Erfahrung im Aufbau eines eCommerce-Shop&nbsp;</li>
	<li style="box-sizing: border-box;">Idealerweise Pharmaerfahrung&nbsp;</li>
	<li style="box-sizing: border-box;">“Growth-Mindset” und die Fähigkeit Dinge voranzutreiben&nbsp;</li>
	<li style="box-sizing: border-box;">Fließende Deutsch-&nbsp; und Englisch-Kenntnisse</li>
</ul>

Rahmendaten: 
Start: asap, spätestens zum 15.10.2022 
Dauer: 6 Monate 
Auslastung: mind. 30 Stunden/Woche, Vollzeit präferiert 
Einsatzort: remote, gelegentlich Vorort&nbsp;

&nbsp;

&nbsp;
</div>

Digital Marketing Manager (m/w/d)

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Einer unserer Pharma-Kunden in Deutschland sucht aktuell freiberufliche Unterstützung als: 
&nbsp; 
Interim Paralegal (M/W/D) 
&nbsp; 
Aufgaben:

<ul>
	<li style="list-style-position:inside">Betreuung von Klassischen &nbsp;„Paralegal“ Aufgaben </li>
	<li style="list-style-position:inside">Eigenständige Betreuung von einfachen Vertragsthemen, Pflege einer Vertragsdatenbank und Einfache Rechtsberatung</li>
	<li style="list-style-position:inside">Beratende Unterstützung von Nicht-Juristen bei der Nutzung von internen Tools/ Templates zu juristischen Themen </li>
	<li style="list-style-position:inside">Mitarbeit bei komplexen juristischen Sachverhalten, gemeinsam mit&nbsp;einem erfahrenen Rechtsanwalt&nbsp;</li>
	<li style="list-style-position:inside">Pflege von Rechnungen/ Zahlungsvorgängen der Rechtsabteilung</li>
</ul>

&nbsp;Qualifikation:

<ul>
	<li style="list-style-position:inside">Mehrjährige Berufserfahrung als Assistent oder ReNo in einem juristischen Umfeld oder Wirtschaftsjurist</li>
	<li style="list-style-position:inside">Pharmaerfahrung</li>
	<li style="list-style-position:inside">Konzernerfahrung von Vorteil </li>
	<li style="list-style-position:inside">Deutsch und Englisch fließend</li>
	<li style="list-style-position:inside">Bereitschaft sich zügig in komplexe Strukturen und Vorgänge einzuarbeiten</li>
	<li style="list-style-position:inside">Eigenverantwortliches Arbeiten</li>
</ul>

Rahmendaten: 
Start: sofort, spätestens zum 15.10.2022 
Dauer: 13 Monate 
Auslastung: 3-5 Tage/Woche 
Einsatzort: Remote und Onsite – Einarbeitung idealerweise vor Ort, danach flexibel 

&nbsp;
</div>

Interim Paralegal

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
<div style="border-width:100%">
<div style="width:7.5in">
<div style="width:7.5in">Project Manager (M/W/D) 
&nbsp; 
Tasks:
<ul style="unicode-bidi:embed" type="disc">
	<li style="vertical-align:middle">Leads or contributes to selected cross-functional and high priority projects in alignment to GCS strategy, from start to completion.</li>
	<li style="vertical-align:middle">Stakeholder engagement</li>
	<li style="vertical-align:middle">Planning and support running of steering committee</li>
	<li style="vertical-align:middle">Review the project plan and keep it updated</li>
	<li style="vertical-align:middle">Prepare and update status and risk</li>
	<li style="vertical-align:middle">Collaborate and plan for change management (communication plan)</li>
	<li style="vertical-align:middle">Adherence to Novartis standards and Values &amp; Behaviors, in particular, quality, ethical, health, safety, and environment standards (HSE), and information security standards (ISEC)</li>
</ul>
&nbsp; 
&nbsp; 
Qualifications:

<ul style="unicode-bidi:embed" type="disc">
	<li style="vertical-align:middle">Degree in science, engineering or equivalent</li>
	<li style="vertical-align:middle">5 years of practical experience in chemical / pharmaceutical industry </li>
	<li style="vertical-align:middle">Data / Analytical/IT Experience (IT Project Management is good)</li>
	<li style="vertical-align:middle">Supply Chain / Master Data Knowledge</li>
	<li style="vertical-align:middle">Good knowledge about the Drug Development process</li>
	<li style="vertical-align:middle">Basic project management, good organization and planning skills</li>
	<li style="vertical-align:middle">Knowledge of relevant regulations (e.g. GMP, HSE etc.) and Novartis specific standards</li>
	<li style="vertical-align:middle">Demonstrates problem-solving and idea generation skills</li>
	<li style="vertical-align:middle">Good presentation skills</li>
	<li style="vertical-align:middle">Very good communication, negotiation and interpersonal skills</li>
	<li style="vertical-align:middle">Ability to work in interdisciplinary team</li>
	<li style="vertical-align:middle">Languages: Fluent in English</li>
</ul>
&nbsp; 
&nbsp; 
Requirements: 

<ul style="unicode-bidi:embed" type="disc">
	<li style="vertical-align:middle">Start: ASAP</li>
	<li style="vertical-align:middle">Duration: 14.09.2023</li>
	<li style="vertical-align:middle">Capacity: Full time on-site</li>
	<li style="vertical-align:middle">Location: Basel, Switzerland</li>
</ul>
&nbsp;</div>
</div>
</div>
</div>

Project Manager

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
<div>One of our pharmaceutical clients in Baden Württemberg is currently looking for freelance support as a: 
 
Clinical Supply Manager (M/W/D) 
 
Tasks:
<ul>
	<li style="margin-left:8px; margin-bottom:11px;list-style-position:inside">Consulting for supply activities for clinical trials</li>
	<li style="margin-left:8px; margin-bottom:11px;list-style-position:inside">Create future commercial supply utilising sound forecasting tools and methodologies</li>
	<li style="margin-left:8px; margin-bottom:11px;list-style-position:inside">Production planning and distribution for clinical trials</li>
	<li style="margin-left:8px; margin-bottom:11px;list-style-position:inside">Provision for supplies for IMP clinical trials with IMP</li>
	<li style="margin-left:8px; margin-bottom:11px;list-style-position:inside">Set up successful relationships with vend. (Manufacturing, Distribution, Packaging, Supply)</li>
	<li style="margin-left:8px; margin-bottom:11px;list-style-position:inside">Work with different departments like Clinical Operations, CMC, Medical, Quality, and different project teams on all aspects of supply </li>
</ul>
 
Qualification:

<ul>
	<li style="margin-left:8px; margin-bottom:11px;list-style-position:inside">Degree in life science or medical area</li>
	<li style="margin-left:8px; margin-bottom:11px;list-style-position:inside">At least 3-5 years of experience in clinical supply management</li>
	<li style="margin-left:8px; margin-bottom:11px;list-style-position:inside">Profound Experience in setting up vendor relationships</li>
	<li style="margin-left:8px; margin-bottom:11px;list-style-position:inside">Establishing, maintaining, and developing successful relationships with vendors</li>
	<li style="margin-left:8px; margin-bottom:11px;list-style-position:inside">Experienced Clinical Trial Management Know-How</li>
	<li style="margin-left:8px; margin-bottom:11px;list-style-position:inside">Prior experience in biopharmaceutical industry</li>
	<li style="margin-left:8px; margin-bottom:11px;list-style-position:inside">Excellent knowledge of cGMP requirements and GMP packaging</li>
	<li style="margin-left:8px; margin-bottom:11px;list-style-position:inside">Very good understanding of the development of GDP-compliant transport processes</li>
	<li style="margin-left:8px; margin-bottom:11px;list-style-position:inside">Preparation and Implementation of the current GDP processes &amp; SOPs training</li>
	<li style="margin-left:8px; margin-bottom:11px;list-style-position:inside">Must have: English&nbsp; (German nice to have)</li>
</ul>
 
Framework data: 
Start: asap, latest 1.10.22 
Duration: 6 months + 
Workload: 30 h 
Location: 90 % remote and max 10 % on site (flexible)</div>
</div>

Clinical Supply Manager

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Einer unserer Medizintechnik-Kunden in Deutschland sucht aktuell freiberufliche Unterstützung als: 
&nbsp; 
Projektleiter für Entwicklungsprojekte (M/W/D) 
&nbsp; 
Aufgaben:

<ul>
	<li style="list-style-position:inside">Gesamtverantwortung für umfangreiche, komplexe Geräte-Entwicklungsprojekte im Bereich Medizintechnik und Diagnostik</li>
	<li style="list-style-position:inside">Geräteentwicklung (Diagnostik) nach ISO 13485</li>
	<li style="list-style-position:inside">Betreuung aller Disziplinen Software, Mechanik, Elektronik</li>
	<li style="list-style-position:inside">Projektplanung, Projektcontrolling, Budget, Kommunikation mit Projektleitern beim Kunden, Zusammenarbeit mit dem Entwicklungsleiter</li>
	<li style="list-style-position:inside">Planung und Umsetzung der Projekte, von der Konzeption bis zur Serienreife</li>
	<li style="list-style-position:inside">Steuerung, Moderation und Zielfokussierung der interdisziplinären Teams</li>
	<li style="list-style-position:inside">Enge Zusammenarbeit mit Kunden zur Erarbeitung von Anforderungen an die Geräte &nbsp;</li>
	<li style="list-style-position:inside">Eigenverantwortliche Planung &amp; Controlling hinsichtlich Kosten, Zeit, Ressourcen sowie der Kundenspezifikationen </li>
</ul>

&nbsp;Qualifikation:

<ul>
	<li style="list-style-position:inside">Abgeschlossenes, technisches oder naturwissenschaftliches Studium </li>
	<li style="list-style-position:inside">Mehrjährige Erfahrung als Projektleiter (m/w/x) oder Technical Lead von Entwicklungsprojekten im industriellen Umfeld sowie erfolgreiche&nbsp; &nbsp; &nbsp; &nbsp;Projektumsetzung bis zur Serienreife</li>
	<li style="list-style-position:inside">Erste Erfahrungen mit sowie Begeisterung für agile Entwicklungsmethoden</li>
	<li style="list-style-position:inside">Kenntnisse im Bereich Medizintechnik oder Diagnostik von Vorteil </li>
	<li style="list-style-position:inside">Geschick für Kommunikation sowie Führung und Motivation von MitarbeiterInnen im Rahmen von interdisziplinären Projekten</li>
	<li style="list-style-position:inside">Systematischer, strukturierter und zielorientierter Ansatz zur Projektleitung und Führung des Projektteams</li>
	<li style="list-style-position:inside">Unternehmerische Denkweise sowie Hands-On-Arbeitsweise</li>
	<li style="list-style-position:inside">Sehr gute Deutsch und Englisch Kenntnisse</li>
</ul>

Rahmendaten: 
Start: ab sofort 
Dauer: 6 Monate 
Auslastung: 5 Tage die Woche 
Einsatzort: Onsite am Standort in Baden-Württemberg

&nbsp;
</div>

Projektleiter Entwicklung

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
One of our pharma clients in Switzerland&nbsp;is currently looking for freelance support as:

&nbsp;

Quality Assurance Specialist Lab Systems Qualification (M/W/D) 
&nbsp; 
Tasks:

<ul>
	<li>Responsible for quality related commissioning and qualification (C&amp;Q)) activities of laboratory systems.</li>
	<li>Quality&nbsp;Representativein for CAPEX project organization</li>
	<li>Reviews and releases of qualification documents and SOPs.</li>
	<li>Subject Matter Expert (SME)&nbsp;</li>
	<li>Represents QA during the various project phases and ensures that GMP requirements are applied.</li>
	<li>Accountable for the review and approval of qualification/validation documents (e.g. URS, DQ/IQ/OQ/PQ Plans and Reports, CSV documentation.</li>
	<li>Accountable for issues, reviews, or approval of deviation reports, assessments and CAPAs in his area of responsibility.</li>
	<li>Writes or revises SOPs in his area of expertise.</li>
	<li>Represent qualification/validation topics during customer audits and regulatory 
	inspections.</li>
</ul>

&nbsp;Qualification:

<ul>
	<li>Bachelor, Master degree or PhD in biotechnology, chemistry, life science or related field</li>
	<li>Significant experience in the GMP regulated pharmaceutical industry; preferable in a role within a Quality Unit or Strong background in cGMP</li>
	<li>Broad knowledge in qualification of lab equipment and systems</li>
	<li>Experience in interaction with all kind of interfaces within the organization and with regulatory agencies (Swissmedic, FDA etc.)</li>
	<li>Excellent verbal, written and interpersonal communications skills</li>
</ul>

Requirements: 
Start: from now on 
Duration: 6 months+ 
Capacity: 5 days per week 
Location: Visp
</div>

Quality Assurance Specialist Lab Systems Qualification

<div data-wrapper="true" style="font-size:10pt;font-family:Arial;">One of our Biotech Clients in Massachusetts is currently looking for freelance support as:

Qualification Expert (M/F/D) 
&nbsp; 
Tasks:

<ul>
	<li><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Owns all quality related responsibilities for the commissioning and qualification (C&amp;Q)) activities of dedicated new facilities, equipment and utilities related to the GMP manufacturing of biologics &amp; APIs</li>
	<li><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">&nbsp;Representative of Quality in the CAPEX project organization in regards to qualification of facilities, utilities, equipment and systems (incl. computerized systems)</li>
	<li><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Reviews and releases of qualification documents and SOPs.</li>
	<li><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Be a Subject Matter Expert (SME) and provides guidance and recommendations to internal or external customers</li>
</ul>

<div>&nbsp;</div>

&nbsp;Qualification:

<ul>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Bachelor, Master degree or PhD in biotechnology, chemistry, life science or related field</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">More than 5 years of Experience in Biotech area</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">At least 2 years of Experience as QA Qualification/Validation OR 5 years in CQV position</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Knowledge on Drug Product (Filling Line, Isolator, depyro tunnel, Washing machine, autoclave) and related Guidelines (e.g. ASTM, ISPE, GAMP)</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Strong experience with the PQ phase (performance qualification)</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Strong background in cGMPExperience in interaction with all kind of interfaces within the organization and with regulatory agencies (FDA)</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Excellent verbal, written and interpersonal communications skills</li>
</ul>

<div style="list-style-position:inside">&nbsp;</div>

Requirements: 
Start: asap 
Duration: 3 months 
Capacity: 3 days per week 
Location: Massachusetts, fully onsite</div>

Qualification Expert

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
One of our Medtech Clients in San Francisco&nbsp;is currently looking for freelance support as:

B2B2C Manager (M/F/D) 
&nbsp; 
Tasks:

<ul>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Detailing consumer marketing initiatives via HCPs focusing on B2B2C</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Consumer research provided by Consumer Insights Manager</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Defining tone of voice for consumer interaction and aligns between different channels</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Working with Content Strategists to ensure content created by agencies in collaboration with agencies matches strategic direction</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Collaborates with MarCom (communication, campaigns tool usage) &amp; DCSM (infrastructure, tool set-up)</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Manage content provided to HCPs, directed at (potential) consumers on all relevant channels:
	<ul>
		<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Owner Channels: E.g., Advertising materials for patients provided to surgeons</li>
		<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Paid channels: E.g., digital campaigns, offline HCP engagement, customer success program etc.</li>
		<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Earned channels: E.g., Websites of customers etc.</li>
	</ul>
	</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Consult B2B2C Managers in regions and take responsibility for localization of the B2B2C Strategy</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Budget responsibility &amp; roadmap planning&nbsp;</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Roadmap and business requirements ready to be implemented upon completion</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Support strategy refinement &amp; evolution</li>
</ul>

&nbsp;Qualification:

<ul>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Degree in Business Administration, Computer science, engineering, natural science, or related fields</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Profound experience in digital marketing; proven track record of delivery of projects with creative output incl. knowledge of digital marketing methodologies</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Knowledge of agile methodologies</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Experience in Health care and related IT systems</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Experience in acquiring patients for HCPs (or pharma)</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Experience working on various stakeholder levels</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Excellent communication and organization skills</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Nice to have: (Digital) designer capabilities</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Nice to have: Management Consulting experience</li>
</ul>

Requirements: 
Start: asap, latest mid of September 
Duration: 8 months 
Capacity: 3 days per week 
Location: Remote
</div>

B2B2C Manager

<div data-wrapper="true" style="font-size:10pt;font-family:Arial;">One of our Medtech Clients in California&nbsp;is currently looking for freelance support as:

R&amp;D Specialist (M/W/D) 
&nbsp; 
Tasks:

<ul>
	<li style="list-style-position: inside;">Process analysis and identification of improvements</li>
	<li style="list-style-position: inside;">Rollout of new methods, tools and processes including workshop preparation, trainings, and coaching</li>
	<li style="list-style-position: inside;">Further development of design and development processes</li>
	<li style="list-style-position: inside;">Configuration and maintenance of tool landscapes</li>
	<li style="list-style-position: inside;">Ensure process and tool reliability within the teams</li>
	<li style="list-style-position: inside;">Interface management within the cross-functional development teams</li>
	<li style="list-style-position: inside;">Contact person for all questions related to product lifecycle</li>
	<li style="list-style-position: inside;">SOP writing</li>
</ul>

&nbsp;Qualification:

<ul>
	<li style="list-style-position:inside;">Master’s in Software or Hardware Engineering or similar</li>
	<li style="list-style-position:inside;">Knowledge of MDR, FDA QSR</li>
	<li style="list-style-position:inside;">Very good knowledge within software/hardware development</li>
	<li style="list-style-position:inside;">Expert in MS TFS</li>
	<li style="list-style-position:inside;">Excellent coaching skills and mentality</li>
</ul>

Requirements: 
Start: asap, latest October, 1st 
Duration: 7 months 
Capacity: minimum 2 days per week 
Location: California</div>

R&D Specialist

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
One of our medical device clients in the San Francisco Bay Area is currently looking for freelance support as:

&nbsp;

Software Developer (M/W/D) 
&nbsp; 
Tasks:

<ul>
	<li lang="en-GB" style="vertical-align:middle; color:black">Software Development</li>
	<li lang="en-GB" style="vertical-align:middle; color:black">Software Design and Testing</li>
	<li lang="en-GB" style="vertical-align:middle; color:black">Python Programming</li>
	<li lang="en-GB" style="vertical-align:middle; color:black">Working with MS Azure Cloud</li>
	<li lang="en-GB" style="vertical-align:middle; color:black">Cross-functional work with developers, engineers and product owners</li>
</ul>

&nbsp;Qualification:

<ul>
	<li lang="en-GB" style="vertical-align:middle; color:black">Degree in computer science or comparable</li>
	<li lang="en-US" style="vertical-align:middle; color:black">Profound experience as software developer</li>
	<li lang="en-US" style="vertical-align:middle; color:black">Excellent knowledge of Python and Microsoft Azure</li>
	<li lang="en-US" style="vertical-align:middle; color:black">Background in designing and developing cloud-based web applications</li>
	<li lang="en-US" style="vertical-align:middle; color:black">Proven success working with agile, interdisciplinary development teams</li>
	<li lang="en-US" style="vertical-align:middle; color:black">Experience within a regulated environment, preferably medtech or life sciences</li>
</ul>

Requirements: 
Start: asap 
Duration: 8 months 
Capacity: full-time 
Location: remote
</div>

Software Developer

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
One of our mecical device clients in Maryland is currently looking for freelance support as:

Project Lead Medical Devices (M/F/D) 
&nbsp; 
Tasks:

<ul>
	<li style="list-style-position: inside;">Leading the definition of product requirements for packaging, medical devices, delivery systems, e.g. drug/device combination products&nbsp;</li>
	<li style="list-style-position: inside;">Leading the collaboration with external and internal development partners and stakeholders&nbsp;</li>
	<li style="list-style-position: inside;">Provide primary packaging and device expertise in a broader cross-functional drug product development team</li>
	<li style="list-style-position: inside;">Evaluating and challenging technical solutions&nbsp;</li>
	<li style="list-style-position: inside;">Managing and monitoring Human Factors Engineering activities&nbsp;</li>
	<li style="list-style-position: inside;">Leading Risk management activities</li>
	<li style="list-style-position: inside;">Planning and monitoring of design verification activities (in-house)</li>
	<li style="list-style-position: inside;">Leading and authoring technical documentation</li>
	<li style="list-style-position: inside;">Ensuring a high-quality Design History file</li>
	<li style="list-style-position: inside;">Transfer of Design History File to production</li>
</ul>

&nbsp;Qualification:

<ul>
	<li style="list-style-position: inside;">Bachelor’s or Master degree in Packaging Science/Engineering or Mechanical Engineering or University level Engineering education</li>
	<li style="list-style-position: inside;">Good understanding of pharmaceutical/ regulated development in general&nbsp;</li>
	<li style="list-style-position: inside;">Experience in project / program management of complex projects</li>
	<li style="list-style-position: inside;">Considerable experience of managing external suppliers</li>
	<li style="list-style-position: inside;">General understanding of Human Factors Engineering, risk management and clinical studies processes and requirements</li>
</ul>

<div style="list-style-position:inside">Requirements: </div>

<div style="list-style-position:inside">Start: latest october</div>

<div style="list-style-position:inside">Duration: 12 months</div>

<div style="list-style-position:inside">Capacity: 3-5 days per week</div>

<div style="list-style-position:inside">Location: Maryland</div>
</div>

Project Lead Medical Devices

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
One of our medical device clients in California&nbsp;is currently looking for freelance support as:

Regulatory Affairs Manager (M/F/D) 
&nbsp; 
Tasks:

<ul>
	<li style="list-style-position: inside;">Identifies, interprets, and disseminates new regulatory trends, expectations and guidance documents</li>
	<li style="list-style-position: inside;">Responsible for assessment of device changes for regulatory implications</li>
	<li style="list-style-position: inside;">Develops positive and proactive approaches for regulatory activities to ensure customer satisfaction</li>
	<li style="list-style-position: inside;">Ensures compliance with regulations and laws pertaining to company business provides guidance and advice</li>
	<li style="list-style-position: inside;">Leads the identification of regulatory risk areas and develops alternative courses of action</li>
	<li style="list-style-position: inside;">Assesses impact of new regulations and works with the Organization to implement appropriate changes</li>
	<li style="list-style-position: inside;">Independently reviews and approves RA Documents, procedures, SOPs and other documentation with respect to commitments, regulations and filings</li>
	<li style="list-style-position: inside;">Creation and submissions of US FDA pre-submissions, 510(k)s and PMAs for assigned projects 
	&nbsp;</li>
</ul>

Qualification:

<ul>
	<li style="list-style-position: inside;">Several years of experience in regulatory, development, clinical affairs, quality, or program management in IVD, medical device, or pharma industries</li>
	<li style="list-style-position: inside;">Experience with regulatory submissions for IDE, 510(k), PMA and CE Mark</li>
	<li style="list-style-position: inside;">Experience in a supervisory or equivalent project leadership role required</li>
	<li style="list-style-position: inside;">Excellent oral and written communication skills with experience preparing and presenting to groups</li>
	<li style="list-style-position: inside;">Strong organizational skills and attention to detail required 
	&nbsp;</li>
</ul>

Requirements: 
Start: september 
Duration: 6-12 months 
Capacity: min. 4 days per week 
Location: remote
</div>

Regulatory Affairs Manager

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
One of our pharma clients in Massachusetts is currently looking for freelance support as:

&nbsp;

CRA / Dermatology (M/F/D)&nbsp; 
&nbsp; 
Tasks:

<ul>
	<li style="list-style-position: inside;">Conduct all types of monitoring visits (site selection, initiation visits, regular visits and close out visits) and remote monitoring.</li>
	<li style="list-style-position: inside;">Preparation and update of monitoring plans and site initiation presentation</li>
	<li style="list-style-position: inside;">Liaising with clinical trial suppliers and other vendors</li>
	<li style="list-style-position: inside;">Working closely with various internal departments</li>
	<li style="list-style-position: inside;">Preparation of study documents</li>
</ul>

&nbsp;Qualification:

<ul>
	<li style="list-style-position: inside;">Successfully completed degree in natural sciences</li>
	<li style="list-style-position: inside;">At least 2 years of experience as a CRA</li>
	<li style="list-style-position: inside;">Experience in the field of dermatology</li>
	<li style="list-style-position: inside;">Very good knowledge of Good Clinical Practice/ICH</li>
	<li style="list-style-position: inside;">Hands-on mentality, solution oriented</li>
	<li style="list-style-position: inside;">Business fluent in German &amp; English</li>
	<li style="list-style-position: inside;">Requirements: </li>
</ul>

Requirements:

Start: asap, latest october 
Duration: min. 3 months 
Capacity: min. 2 days per week 
Location: remote + center visits
</div>

Clinical Research Associate

<div data-wrapper="true" style="font-size:10pt;font-family:Arial;">One of our pharma&nbsp;clients is currently looking for freelance support as:

Quality Engineer (M/W/D) 
&nbsp; 
Tasks:

<ul>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Development and Support of the current Quality Assurance department</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Assuring Quality Compliance with the current regulations</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Leading and participating in all current Quality projects</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Training of staff in QA activities</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Review of Quality related documents and authorizing them</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">CAPA and Deviation Management and Complaint Handling</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Deviations and Root-Cause-Analysis</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Analyzing and compromising of statistical data for Production and respective processes</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Communication within all relevant departments</li>
</ul>

&nbsp;Qualification:

<ul>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Degree in a technical field</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Broad experience in GMP regulated environment</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Knowledge in Process Validation</li>
	<li style="list-style-position: inside;"><span style="-webkit-text-stroke-width:0px; color:#000000; display:inline !important; float:none; font-style:normal; font-variant-caps:normal; font-variant-ligatures:normal; font-weight:400; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px">Knowledge in Project Management tools</li>
</ul>

Requirements: 
Start: latest november&nbsp; 
Duration: 6 months 
Capacity: 4-5 days per week 
Location: California</div>

Quality Engineer

<div data-wrapper="true" style="font-size:10pt;font-family:Arial;">One of our Biotech Clients in Maryland&nbsp;is currently looking for freelance support as:
&nbsp;
Technical Project Manager (M/W/D) &nbsp; Tasks:
<ul><li style="list-style-position: inside;">Project management from the concept phase to commissioning</li><li style="list-style-position: inside;">Coordination and project management, as well as interdisciplinary teamwork with various stakeholders</li><li style="list-style-position: inside;">Interface function between suppliers and internal requirements in life science / diagnostics / pharmaceuticals</li><li style="list-style-position: inside;">Responsible project management in the area of:<ul><li style="list-style-position: inside;">PLC programming as well as commissioning</li><li style="list-style-position: inside;">Design of electrical hardware</li><li style="list-style-position: inside;">Computerized process control systems and conceptual design of computer systems Integration of in-process controls (e.g. vision systems)</li><li style="list-style-position: inside;">Integration of robotics and handling technology, safety technology, bus system/plant interfaces and drive systems and various interfaces</li></ul></li></ul>
&nbsp;Qualification:
<ul><li style="list-style-position: inside;">Electrical or automation engineer or equivalent</li><li style="list-style-position: inside;">3 years + experience working with complex automated equipment, preferably in the pharmaceutical or other regulated industries</li><li style="list-style-position: inside;">Experience with computer systems, programming PLC source code from standard platforms (for example Siemens S7 / TIA Portal)</li><li style="list-style-position: inside;">Experience in programming interfaces, drive technology and vision systems</li><li style="list-style-position: inside;">Ability to work effectively in interdisciplinary teams</li><li style="list-style-position: inside;">Structured way of working and high degree of reliability as well as independence</li><li style="list-style-position: inside;">Solution-oriented even in complex situations</li><li style="list-style-position: inside;">Nice to have: Experience in the field of pharmacy, GMP or chemical environment</li></ul>
Requirements: Start: asap, latest 09.15.22 Duration: 6 months + Capacity: 3-5 days per week Location: onsite and remote</div>

Technical Project Manager

<div data-wrapper="true" style="font-size:10pt;font-family:Arial;">Einer unserer &nbsp;Pharma-Kunden in Hessen&nbsp;sucht aktuell freiberufliche Unterstützung als: 
&nbsp; 
QP §15.1 AMG&nbsp;(M/W/D) 
&nbsp; 
Aufgaben:

<ul>
	<li>Freigabe von Chargen zum Inverkehrbringen von Arzneimitteln</li>
	<li>Auswertung der Chargenprotokolle</li>
	<li>Reklamationsbearbeitung</li>
	<li>CAPA Management&nbsp;</li>
	<li>Beratung Hinsichtlich Reklamationen&nbsp;</li>
	<li>Deviation und Risk Management</li>
</ul>

Qualifikation:

<ul>
	<li>Sachkundige Person/ QP nach §14 AMG</li>
	<li>Erfahrung im Bereich Solida / Semi-Solida / Liquida&nbsp;</li>
	<li>Sehr gute Kenntnisse der aktuellen Standards und Vorschiften (GMP)</li>
	<li>Gute Deutsch- und Englischkenntnisse&nbsp;</li>
</ul>

Rahmendaten: 
Start: Ab sofort / Spätestens 01.10.22 
Dauer: 6 Monate 
Auslastung: 2-3 Tage die Woche 
Einsatzort: Vor Ort &amp; remote&nbsp;</div>

QP §15.1 AMG

<div data-wrapper="true" style="font-size:10pt;font-family:Arial;">Einer unserer Medizintechnik-Kunden in Deutschland sucht aktuell freiberufliche Unterstützung als: 
&nbsp; 
Online Marketingmanager (M/W/D) 
&nbsp; 
Aufgaben:

<ul>
	<li>Beratung bei der Erstellung einer geeigneten Kampagne für höhere Markenbekanntheit</li>
	<li>Erstellung eines Agenturbriefings</li>
	<li>Auswahl einer geeigneten Werbeagentur für Online Marketing via Mail und Social Media</li>
	<li>Professionelle Begleitung, z.B. bei der Chemistry Session</li>
</ul>

&nbsp;Qualifikation:

<ul>
	<li>Erfahrung in der Zusammenarbeit mit Werbeagenturen, Markenbildung und Social Media</li>
	<li>Besondere Kenntnisse in einer hochregulierten Branche</li>
</ul>

Rahmendaten: 
Start: asap 
Dauer: 4 Monate + 
Auslastung: 2-3 Tage die Woche 
Einsatzort: remote</div>

Online Marketingmanager

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
<div>Einer unserer Schweizer&nbsp;Medizintechnik-Kunden sucht aktuell freiberufliche Unterstützung als:&nbsp; 
 
Embedded C++ Experte (M/W/D)&nbsp; 
 
Aufgaben:
<ul>
	<li style="list-style-position:inside">Programmierungen in C++ / UML im Embedded Softwareumfeld</li>
	<li style="list-style-position:inside">Verfassen von Anforderungen</li>
	<li style="list-style-position:inside">Erstellung und Durchführung von Integrationstests, Unit Tests</li>
	<li style="list-style-position:inside">Code Implementierung</li>
	<li style="list-style-position:inside">Analyse und Bewertung von Code Designs </li>
</ul>
 
Qualifikation:

<ul>
	<li style="list-style-position:inside">Start: asap // Dauer: 6 Monate + // Auslastung: Vollzeit vor Ort</li>
	<li style="list-style-position:inside">Studium im Bereich Software Engineering oder vergleichbar</li>
	<li style="list-style-position:inside">Erfahrung im Embedded Umfeld, Embedded Linux</li>
	<li style="list-style-position:inside">Solide Kenntnisse im Umgang mit IBM Rhapsody wünschenswert</li>
	<li style="list-style-position:inside">Deutsch + Englisch fließend</li>
</ul>
 
Rahmendaten:&nbsp;

<ul>
	<li style="list-style-position:inside">Start: ab sofort</li>
	<li style="list-style-position:inside">Dauer: 6 Monate +</li>
	<li style="list-style-position:inside">Auslastung: Vollzeit vor Ort</li>
</ul>
</div>
</div>

Embedded C++ Experte

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Einer unserer Medizintechnik-Kunden in Deutschland sucht aktuell freiberufliche Unterstützung als: 
&nbsp;

Scrum Master (M/W/D) 
&nbsp; 
Aufgaben:

<ul>
	<li style="vertical-align:middle">Verantwortung für bis zu zwei interdisziplinäre agile Teams </li>
	<li style="vertical-align:middle">Unterstützung der Teams, sich kontinuierlich zu verbessern, um eigenverantwortlich die Erreichung der Unternehmensziele voranzutreiben</li>
	<li style="vertical-align:middle">Nutzung agiler Methoden (beispielsweise Scrum, Lean und Kanban), um Verbesserungen voranzutreiben</li>
	<li style="vertical-align:middle">Enge Zusammenarbeit mit den Product Ownern, anderen internationalen Teams und deren Scrum Mastern sowie dem Release Train Engineer&nbsp;</li>
	<li style="vertical-align:middle">Organisation von Team- und Programmevents wie Sprint / Increment Planning, Review, Retrospective und Backlog Refinement</li>
	<li style="vertical-align:middle">Erkennung von potenziellen Hindernissen in den agilen Teams und deren Lösung unter Einbeziehung aller Stakeholder&nbsp;</li>
	<li style="vertical-align:middle">Ansprechpartner für alle Fragen agiler Softwareentwicklung für die agilen Teams und Impulsgeber für die Weiterentwicklung agiler Prozesse&nbsp;</li>
</ul>

&nbsp;

&nbsp;Qualifikation:

<ul>
	<li style="vertical-align:middle">Studium der Informatik, einer anderen Ingenieurswissenschaft oder vergleichbare Qualifikationen</li>
	<li style="vertical-align:middle">mehrjährige Erfahrung als Scrum Master in der Softwareentwicklung, idealerweise in komplexen Umgebungen mit mehreren agilen Teams und in Kombination mit System- / Hardwareentwicklung.</li>
	<li style="vertical-align:middle">Azure DevOps, Jira oder vergleichbare Tools&nbsp;</li>
	<li style="vertical-align:middle">gute Methodenkenntnisse und entsprechende Zertifizierung z.B. als Certified Scrum Professional, Certified Scrum Master oder Certified Team Coach</li>
	<li style="vertical-align:middle">Gute Deutsch- und Englischkenntnisse</li>
</ul>

&nbsp;

Rahmendaten: 
Start: 01.08.2022 / flexibel 
Dauer: 24 Monate 
Auslastung: 4-5 Tage / Woche 
Einsatzort: vor Ort&nbsp;

&nbsp;
</div>

Scrum Master

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">For one of our Pharma clients we are seeking freelance support as: 
 
Clinical Research Associate USA (M/F/D) 
 
Tasks:
<ul>
	<li style="list-style-position:inside">Clinical monitoring in current studies (phase 1)</li>
	<li style="list-style-position:inside">Study Preparation / Study Start up </li>
	<li style="list-style-position:inside">Qualification &amp; Initiation Visits</li>
	<li style="list-style-position:inside">Submission processes (preparation of ethics submissions)</li>
	<li style="list-style-position:inside">Supervision of studies</li>
	<li style="list-style-position:inside">Preparation of study documents</li>
</ul>
 
Qualification:

<ul>
	<li style="list-style-position:inside">Successfully completed degree in natural sciences</li>
	<li style="list-style-position:inside">Several years of CRA experience </li>
	<li style="list-style-position:inside">Experience in the field of oncology</li>
	<li style="list-style-position:inside">Hands-on mentality, solution oriented</li>
	<li style="list-style-position:inside">Willingness to travel (at the end of the year) </li>
	<li style="list-style-position:inside">Fluent in English</li>
</ul>
 
Requirements:

<ul>
	<li style="list-style-position:inside">Start: immediately&nbsp; </li>
	<li style="list-style-position:inside">Duration: 12 months</li>
	<li style="list-style-position:inside">Workload: 30 - 40 hours per week, remote&amp;onsite</li>
</ul>
</div>

CRA USA

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
<div>Einer unserer Pharma-Kunden in Deutschland sucht aktuell freiberufliche Unterstützung als: 
 
Clinical Research Associate Deutschland / Onkologie (M/F/D) 
 
Aufgaben:
<ul>
	<li style="margin-top:20px; margin-left:45px;list-style-position:inside">Klinisches Monitoring bei aktuellen Studien (Phase 2-3) </li>
	<li style="margin-left:45px;list-style-position:inside">Studien Vorbereitung / Study Start up </li>
	<li style="margin-left:45px;list-style-position:inside">Qualification &amp; Initiation Visits </li>
	<li style="margin-left:45px;list-style-position:inside">Einreichungsprozesse (Vorbereitung Ethikeinreichungen) </li>
	<li style="margin-left:45px;list-style-position:inside">Betreuung der Studien </li>
	<li style="margin-bottom:20px; margin-left:45px;list-style-position:inside">Erstellung von Studiendokumenten </li>
</ul>
 
Qualifikation:

<ul>
	<li style="margin-top:20px; margin-left:45px;list-style-position:inside">Erfolgreich abgeschlossenes Naturwissenschaftliches Studium </li>
	<li style="margin-left:45px;list-style-position:inside">Mehrjährige CRA Erfahrung </li>
	<li style="margin-left:45px;list-style-position:inside">Erfahung mit Risk- based Monitoring (RBM) </li>
	<li style="margin-left:45px;list-style-position:inside">Erfahrung im Bereich Onkologie </li>
	<li style="margin-left:45px;list-style-position:inside">Hands-on Mentalität, Lösungsorientiert </li>
	<li style="margin-left:45px;list-style-position:inside">Reisebereitschaft DE </li>
	<li style="margin-bottom:20px; margin-left:45px;list-style-position:inside">Verhandlungssicher in Deutsch &amp; Englisch </li>
</ul>
 
Rahmendaten: 

<ul>
	<li style="margin-top:20px; margin-left:45px;list-style-position:inside">Start: asap, latest October 2022</li>
	<li style="margin-left:45px;list-style-position:inside">Dauer: 12 Monate plus </li>
	<li style="margin-left:45px;list-style-position:inside">Auslastung: 20-25 Stunden pro Woche remote</li>
</ul>
</div>
</div>

CRA Onkologie

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">Einer unserer Pharma-Kunden in Deutschland sucht aktuell freiberufliche Unterstützung als: &nbsp; Experte Anlagen- und Raumqualifizierung (M/W/D) &nbsp; Aufgaben:
<ul><li>Begleitung d. versch. Projektphasen (konzeptionelles Design &amp; Detaildesign u.a.)</li><li>Qualifizierung von Produktionsanlagen f. feste Darreichungsformen</li><li>Qualifizierung von Reinräumen Klasse D</li></ul>
&nbsp;Qualifikation:
<ul><li>mehrjährige Erfahrung im Bereich Anlagen- und Raumqualifizierung</li><li>langjährige Pharma- oder veterinärmedizinische Erfahrung</li><li>fundierte Erfahrung im Bereich Design Qualification</li><li>Deutsch must, Englisch nice to have</li></ul>
Rahmendaten: Start: 01.09.-01.10.2022 Dauer: 12 Monate Auslastung: 2-3 Tage die Woche Einsatzort: Kiel</div>

Experte Anlagen- und Raumqualifizierung

<div data-wrapper="true" style="font-family:Arial; font-size:10pt">Einer unserer Pharma-Kunden in Deutschland sucht aktuell freiberufliche Unterstützung als: &nbsp; Leitung Qualitätskontrolle (M/W/D) &nbsp; Aufgaben:
<ul><li>Freigaben, Analysen und Abweichungsmanagement im Bereich Qualitätskontrolle</li><li>Fachlicher Ansprechpartner für ein 15-köpfiges Team</li><li>Implementierung von Analysetechniken inkl. Wissenstransfer in Bestandsabteilung</li><li>Bearbeitung von Abweichungen</li><li>Lieferanten- und Materialbewertungen sowie Einführung von neuen Materialien</li></ul>
&nbsp;Qualifikation:
<ul><li>Langjährige Erfahrung in pharmazeutischer Industrie</li><li>Expertise mit der Qualitätskontrolle im Kontext fester Darreichungsformen</li><li>Deutsch und Englisch in Wort und Schrift</li><li>Nice to have: Trackwise-Erfahrung</li></ul>
Rahmendaten: Start: Anfang Oktober, spät Mitte Oktober Dauer: 12+ Monate Auslastung: 4-5 Tage / Woche Einsatzort: vor Ort im Großraum Stuttgart</div>

Leitung Qualitätskontrolle

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">One of our Pharma clients in Switzerland&nbsp;is currently looking for temporafy support as:
&nbsp;
QA Manager Cleaning Validation (M/W/D) &nbsp; Tasks:
<ul><li style="list-style-position: inside;">Ensure QA oversight for Cleaning Design activities to a Large Scale Cell Culture Mammalian Facility</li><li style="list-style-position: inside;">Define &nbsp;and review CIP strategy approach with the design and CQV team according to Lonza procedure and in compliance with regulatory guidance.</li><li style="list-style-position: inside;">Technical lead of cleaning validation teams including communication with customers, as appropriate.</li><li style="list-style-position: inside;">Support / review / approve QC cleaning studies.</li></ul>
<div>&nbsp;Qualification:</div>
<ul><li style="list-style-type:none;list-style-position:inside">&nbsp;</li><li style="list-style-position:inside;">Bachelor, Master degree or PhD in Analytical Science, biotechnology, chemistry or related field</li><li style="list-style-position:inside;">Significant experience in the GMP regulated pharmaceutical industry; preferable in a role within the Quality Unit (QA, QC)</li><li style="list-style-position:inside;">Strong background in cGMP</li><li style="list-style-position:inside;">Broad knowledge in cleaning validation of biopharmaceuticals &amp;Biologics</li><li style="list-style-position:inside;">Experience in interaction with all kind of interfaces within the organization and with regulatory agencies (Swissmedic, FDA etc.)</li><li style="list-style-position:inside;">Excellent verbal, written and interpersonal communications skills</li><li style="list-style-position:inside;">Fluency in English, German would be an advantage</li></ul>
<div>Requirements: Start: ASAP Duration: 6 months Capacity: 5 days per week Location: Switzerland</div></div>

QA Manager Cleaning Validation

<div data-wrapper="true" style="font-size:10pt;font-family:Arial;"><div>Technical Administration and Configuration of Project and Portfolio Management Tool</div>

<div>&nbsp;</div>

<div>Project description:</div>

<div>&nbsp;
<ul>
	<li style="list-style-position:inside">Implementation and configurations of standard Project and Portfolio Management tools (Clarizen) in regards to workflow configurations, layouts, dashboards, custom panels, reports etc. thus aim to solve business challenges while enhancing the user experience with automation and streamlined solution</li>
	<li style="list-style-position:inside">Technical documentation, manuals, training concepts for project management tools and conduct trainings</li>
	<li style="list-style-position:inside">Contribution to the analysis and development of technical and process enhancements within related tools</li>
	<li style="list-style-position:inside">Identification of tools customization needs and management of implementation through prioritization</li>
</ul>
 
Required project methods and tools: 
&nbsp;
<ul>
	<li style="margin-top:4px; margin-bottom:4px;list-style-position:inside">PMO-Tools (preferably Clarizen)</li>
	<li style="margin-top:4px; margin-bottom:4px;list-style-position:inside">JavaScript, HTML und CSS</li>
</ul>

<div style="list-style-position:inside; margin-bottom:4px; margin-top:4px">&nbsp;</div>

<div style="list-style-position:inside; margin-bottom:4px; margin-top:4px">
<div>Project framework: 
&nbsp;</div>

<ul>
	<li style="list-style-position:inside">Project duration: 01.09.2022 – 23.12.2022; optionally Project extension until 31.03.2023 </li>
	<li style="list-style-position:inside">Average 20 Project days per month </li>
	<li style="list-style-position:inside">100% remote</li>
</ul>
</div>
</div></div>

Technical Administrator

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Einer unserer Medizintechnik-Kunden in Deutschland sucht aktuell freiberufliche Unterstützung als: 
&nbsp; 
Consultant Value Management (M/W/D) 
&nbsp; 
Aufgaben:

<ul>
	<li>Strategische Beratung im Bereich&nbsp;Value Management</li>
	<li>Wertanalyse der Geschäftsfelder und Formulieren von Zielen und Sollvorgaben</li>
	<li>Aktiv zum Voranbringen des Themas Innovation Management beitragen</li>
	<li>Beratung in den Bereich Cost Management, Change Management, Potentialdetektion</li>
	<li>Gegebenefalls Entwickelng und Halten von Workshops</li>
</ul>

&nbsp;Qualifikation:

<ul>
	<li>Nachgewiesene Erfahrung und Erfolge im Bereich Value Management in der High-Tech Branche</li>
	<li>
	<div>Erfahrung im Bereich Projektleitung, Kostensenkung, Innovation</div>
	</li>
	<li>Ganzheitliches/analytisches Denken, Kundenorientierung, Interdisziplinäres, Konzeptionsstärke&nbsp;</li>
	<li>Life Science Erfahrung wünschenswert</li>
	<li>Deutsch und Englisch verhandlungssicher</li>
</ul>

Rahmendaten: 
Start: 01.09.2022, spätestens 01.10.2022 
Dauer: 6 Monate + 
Auslastung: 2-3 Tage die Woche 
Einsatzort: Remote und geringfügig vor Ort
</div>

Consultant Value Management

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">Einer unserer Biotech-Kunden in Deutschland sucht aktuell freiberufliche Unterstützung als: &nbsp; Projektingenieur Anlagenmodernisierung (M/W/D) &nbsp; Aufgaben:
<ul><li>Modifikation von Bestandsanlage</li><li>Koordination der technischen Seite inkl. Verfahrenstechnik</li><li>Beschaffung von Equipment bei bereits bekannten Stammlieferanten des Kunden</li><li>Technische Prüfung der Angebote</li><li>Stakeholdermanagement</li></ul>
&nbsp;Qualifikation:
<ul><li>Erfahrung im Bereich Projektengineering</li><li>SAP-Kenntnisse von Vorteil</li><li>Expertise in Pharma/Biotech o. Lebensmittelindustrie</li><li>Deutsch in Wort und Schrift</li></ul>
Rahmendaten: Start: 01.10.2022, spät. November Dauer: 4 Monate&nbsp; Auslastung: 3-5 Tage die Woche, je nach Projektstatus Einsatzort: Frankfurt &amp; remote, je nach Projektstatus</div>

Projektingenieur Anlagenmodernisierung

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Einer unserer Medizintechnik-Kunden im Großraum Aachen&nbsp;sucht aktuell freiberufliche Unterstützung als: 
&nbsp; 
Prozessingenieur (M/W/D) 
&nbsp; 
Aufgaben:

<ul>
	<li>Optimierung bestehender Produktionsprozesse hinsichtlich Effizienz&nbsp;und Effektivität</li>
	<li>Prozesskontrolle, Fehleranalyse und Umsetzung von Lösungen</li>
	<li>CAPA Management</li>
	<li>Weiterentwicklung der Fertigungstechnik</li>
	<li>Prototypenbau, Erstmusterung und Dokumentationserstellung</li>
	<li>Erstellung von Change-Anträgen</li>
	<li>Überführung von Baugruppen und Produkten aus der Entwicklung in&nbsp;die Serienfertigung</li>
</ul>

&nbsp;Qualifikation:

<ul>
	<li>Erfolgreich abgeschlossenes Studium im Bereich Technik, Naturwissenschaften oder eine vergleichbare Qualifikation</li>
	<li>Mehrjährige Berufserfahrung im industriellen Produktionsumfeld, vorzugsweise in der Medizintechnik</li>
	<li>Sehr gutes analytisches Denkvermögen mit einem starken Willen zur Optimierung von Prozessen und der Fähigkeit, komplexe Sachverhalte einfach darzustellen und zu kommunizieren</li>
	<li>Eigenmotivierte, selbstständige, strukturierte, zielorientierte&nbsp;Arbeitsweise</li>
	<li>Konversationssichere Englischkenntnisse in Wort und Schrift</li>
</ul>

Rahmendaten: 
Start: asap 
Dauer: 6 Monate+ 
Auslastung: 5 Tage die Woche 
Einsatzort: Großraum Aachen

&nbsp;

&nbsp;
</div>

Process Engineer

<div data-wrapper="true" style="font-size:10pt;font-family:Arial;"><div>Einer unserer Medizintechnik-Kunden in der Schweiz sucht aktuell freiberufliche Unterstützung als: 
 
Software Test Engineer (M/W/D) 
&nbsp; 
Aufgaben: 
<table cellspacing="0" class="Table" style="border-collapse:collapse" summary="" title="">
	<tbody>
		<tr>
			<td colspan="2" style="padding:5px 5px 5px 5px; vertical-align:top; width:593px">
			<ul>
				<li style="list-style-position:inside">Kommunikation mit Projektbeteiligten, um die Anforderungen zu verstehen und daraus Teststrategien abzuleiten</li>
				<li style="list-style-position:inside">Erstellung und Pflege von Testkonzepten / -strategien zum Testen der SW von Medizinprodukten</li>
				<li style="list-style-position:inside">Erstellung, Pflege und Durchführung von Testplänen auf System-, Integrations- und Unit-Testebene</li>
				<li style="list-style-position:inside">Betreuung des Projektteams bei der Erstellung/Automatisierung von Testszenarien auf System-, Integrations- und Unit-Testebene</li>
				<li style="list-style-position:inside">Informieren aller interessierten Stakeholder über die Testergebnisse und den Status und die Einhaltung von Schlüsselmetriken und statischen Tests</li>
				<li style="list-style-position:inside">Mithilfe bei QA-Aufgaben </li>
			</ul>
			</td>
			<td style="padding:0cm 0cm 0cm 0cm; width:25px">&nbsp;</td>
		</tr>
		<tr>
			<td style="padding:0cm 0cm 0cm 0cm; width:25px">&nbsp;</td>
			<td colspan="2" style="padding:5px 5px 5px 5px; vertical-align:top; width:593px">Qualifikation: 
			<ul>
				<li style="list-style-position:inside">Erfahrung in der Erstellung, Pflege, Implementierung und Ausführung von Testszenarien (Entwurfs-, System-, Integrations- und Einheitstests)</li>
				<li style="list-style-position:inside">Gute Kenntnisse der regulatorischen Anforderungen im medizinischen Umfeld</li>
				<li style="list-style-position:inside">Erfahrung in der Testautomatisierung</li>
				<li style="list-style-position:inside">Erfahrung in der Erstellung von Testkonzepten/Strategien</li>
				<li style="list-style-position:inside">Fließende Sprachkenntnisse in Deutsch und Englisch</li>
			</ul>
			</td>
		</tr>
		<tr>
			<td style="padding:0cm 0cm 0cm 0cm; width:25px">&nbsp;</td>
			<td style="padding:0cm 0cm 0cm 0cm; width:563px">&nbsp;</td>
			<td style="padding:0cm 0cm 0cm 0cm; width:24px">&nbsp;</td>
		</tr>
	</tbody>
</table>
&nbsp; 
Rahmendaten: 

<ul>
	<li style="list-style-position:inside">Start: asap</li>
	<li style="list-style-position:inside">Dauer: 6 Monate +</li>
	<li style="list-style-position:inside">Auslastung: Vollzeit vor Ort</li>
</ul>
</div></div>

Software Test Engineer

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Einer unserer Biotechnologie-Kunden in Deutschland sucht aktuell freiberufliche Unterstützung als: 
&nbsp; 
Controller (M/W/D) 
&nbsp; 
Aufgaben:

<ul>
	<li style="list-style-position: inside;">Reports erstellen für die Geschäftsführung</li>
	<li style="list-style-position: inside;">Budgets und Forecasts erstellen</li>
	<li style="list-style-position: inside;">Analyse der Geschäftsentwicklung, Abweichungsanalysen</li>
	<li style="list-style-position: inside;">Ad-hoc-Analysen, Szenarien ausarbeiten</li>
	<li style="list-style-position: inside;">Digitalisierungsprojekte durchführen</li>
	<li style="list-style-position: inside;">Projektcontrolling ausbauen</li>
</ul>

&nbsp;Qualifikation:

<ul>
	<li lang="de" style="vertical-align:middle">Mind. 2 Jahre Berufs- oder Projekterfahrung im Bereich Controlling</li>
	<li lang="de" style="vertical-align:middle">Verhandlungssicheres Englisch in Wort und Schrift </li>
	<li style="vertical-align:middle">Einschlägige Erfahrung mit BI-Tools </li>
	<li style="vertical-align:middle">Eine selbstständige Arbeitsweise und ein hohes Maß an Ergebnisorientierung werden vorausgesetzt</li>
	<li style="vertical-align:middle">Teamfähigkeit, kommunikatives Auftreten</li>
</ul>

Rahmendaten: 
Start: asap 
Dauer: 3 Monate 
Auslastung: 30 - 40 Std. pro Woche 
Einsatzort:&nbsp;vor Ort (Deutschland&nbsp;+ ggf. mal remote)
</div>

Experte im Controlling

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">Einer unserer Medizintechnik-Kunden in Deutschland sucht aktuell freiberufliche Unterstützung als: &nbsp; Product Manager (M/W/D) &nbsp; Aufgaben:
<ul><li style="box-sizing:border-box;margin-bottom:0.5rem !important;">Identifizierung von Markt- und Technologietrends&nbsp;</li><li style="box-sizing:border-box;margin-bottom:0.5rem !important;">Dokumentation und Beratung zwischen den Business-Units</li><li style="box-sizing:border-box;margin-bottom:0.5rem !important;">Systematische Analyse und Strukturierung der Eingaben und Entwicklung empfohlener Anforderungen</li><li style="box-sizing:border-box;margin-bottom:0.5rem !important;">Entwicklung eines Produktbriefings, einschließlich unerfüllter Bedürfnisse, Zielgruppen, Positionierung, USPs und Preisgestaltung</li><li style="box-sizing:border-box;margin-bottom:0.5rem !important;">Identifizierung von Bedürfnissen und Lösungsmöglichkeiten durch Produktpositionierung</li><li style="box-sizing:border-box;margin-bottom:0.5rem !important;">Wissenstransfer zwischen den Stakeholdern</li><li style="box-sizing:border-box;margin-bottom:0.5rem !important;">Verwaltung von Artikeln, Produktbündeln und Preisen für das zugewiesene Produkt &nbsp;</li></ul>
&nbsp;Qualifikation:
<ul><li style="box-sizing: border-box; margin-bottom: 0.5rem !important;">Nachgewiesene Erfahrungen mit Produktlaunches</li><li style="box-sizing: border-box; margin-bottom: 0.5rem !important;">etablierte Präsentations- und Kommunikationsfähigkeiten</li><li style="box-sizing: border-box; margin-bottom: 0.5rem !important;">Erfahrungen Projektmanagement- und Stakeholder-Management</li><li style="box-sizing: border-box; margin-bottom: 0.5rem !important;">Kenntnisse mit Salesforce und BI Tools</li><li style="box-sizing: border-box; margin-bottom: 0.5rem !important;">Reisebereitschaft Süddeutschland</li><li style="box-sizing: border-box; margin-bottom: 0.5rem !important;">Verhandlungssicheres Englisch in Wort und Schrift</li></ul>
Rahmendaten: 
<div>Start: Asap</div>
<div>Dauer: 12 Monate Auslastung: 5 Tage die Woche Einsatzort: vor Ort &amp; remote</div></div>