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I would like to be included in the K-Recruiting applicant pool. This will give me the opportunity to receive further exciting offers. By being included in the applicant 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.

Apply to join our team.

I would like to be included in the K-Recruiting expert pool. This will give me the opportunity to receive further exciting offers. By being included in the expert 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.

Are you interested in this project?

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" dir="ltr" style="font-family:Arial; font-size:10pt">
Senior V&amp;V Engineer (M/W/D)

&nbsp;

Aufgaben:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="margin: 0cm; line-height: normal;">Leitung, Durchführen und Bewerten von Testmethoden- und Prozessvalidierungen,&nbsp;in besonderen Fällen auch im Rahmen von (Re-) Zertifizierungsprojekten </li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Planung, Durchführung/Koordination und Dokumentation Prozessvalidierungsaktivitäten im Rahmen von Entwicklungsprojekten</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Review der zugehörigen Dokumentation im Rahmen von Entwicklungsprojekten&nbsp; </li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Unterstützung der Fachabteilungen im Rahmen von Behördenrückfragen und Audits </li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Planung, Koordination und Überwachung von mechanischen sowie analytischen Testabläufen bei Validierungen sowie Rohdatenauswertung, Berichterstellung, -prüfung und –freigabe </li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Freigabe von Equipment in den Entwicklungslaboren</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Freigabe und Prüfung der Annual Stabilitätsstudien (Protokoll und Report) bis zur Übergabe</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Entwicklung und Einsatz von Kompetenzen im Bereich Design Control &amp; Risk Management</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Mitarbeit in abteilungsübergreifenden Expertengruppen zum Fachbereich Process Verifizierung &amp; Validierung</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Trending, Auswertungen und Berichterstattungen, sowie Präsentationen von qualitätsrelevanten Daten während der Entwicklungsphase</li>
</ul>

<div style="font-family:&quot;Open Sans&quot;,sans-serif; font-size:15px; line-height:normal; margin-bottom:0cm; margin-left:0cm; margin-right:0cm; margin-top:0cm">&nbsp;</div>

Qualifikation:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Hochschul- / Universitätsabschluss, ggf. Promotion oder vergleichbare Ausbildung</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">&gt;7 Jahre relevante Berufserfahrung</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Produktkenntnisse: Medizinprodukte, Vascular Intervention, Kombinationsprodukte</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Kenntnisse von internationalen, regulatorischen Anforderungen im Bereich Vascular Intervention für Risiko Management , Prozess Verifizierung &amp; Validierung und Testmethodenvalidierungen (u.a. MDR, MDD, QSR, ISO 13485, ISO 14971, ISO 9001, cGxP)</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Six Sigma Green Belt oder ähnlich&nbsp;</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Prozessvalidierung, Testmethodenvalidierung, Equipment Qualifizierung</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">fliessende Deutsch- und Englischkenntnisse</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Kenntnisse mit ERP und PLM Systemen</li>
</ul>

<div style="font-family:&quot;Open Sans&quot;,sans-serif; font-size:15px; line-height:normal; margin-bottom:0cm; margin-left:0cm; margin-right:0cm; margin-top:0cm">&nbsp;</div>

Rahmendaten:&nbsp;

Start: 01.08.2023

Dauer: 10 Monate (bis 31.05.2024) inkl. Option auf Verlängerung&nbsp;

Auslastung: 100 %&nbsp;

Einsatzort: Grossraum Zürich&nbsp;
</div>

Senior V&V Engineer

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" dir="ltr" style="font-family:Arial; font-size:10pt">Einer unserer MedTech-Kunden in Baden-Württemberg sucht aktuell freiberufliche Unterstützung als: &nbsp; Project Manager MDR &nbsp;(M/W/D) &nbsp; Aufgaben: 
<ul><li style="list-style-position:inside">Review und Zusammenstellung von MDR Tech Files- Klasse 1r bis Klasse III </li><li style="list-style-position:inside">Überprüfung der MDR-Konformität aller Dokumente</li><li style="list-style-position:inside">Crossfunctionale Zusammenarbeit mit Regulatory Affairs und Quality Management </li><li style="list-style-position:inside">Mitarbeit Aufbau und Umsetzung MDSAP System </li><li style="list-style-position:inside">Einreichung von Anträgen bei der US-FDA und bei der Beantwortung von Mängeln</li><li style="list-style-position:inside">Aktualisierungen der technischen Unterlagen und Ermittlung der Prüfberichte</li><li style="list-style-position:inside">Klassifizierungsdokumente ausfüllen </li><li style="list-style-position:inside">Koordinieren&nbsp;von Distributoren und Lieferanten &nbsp;</li></ul>
<div>&nbsp; Qualifikation:
<ul><li style="list-style-position:inside">Profunde Erfahrung über MDR-Anforderungen</li><li style="list-style-position:inside">Langjährige Erfahrung in der Medizintechnik (wünschenswert im Bereich Spine &amp; Orthopedics) </li><li style="list-style-position:inside">Erfahrungen Aufbau und Umsetzung von MDSAP-Systemen </li><li style="list-style-position:inside">Fundierte Kenntnisse mit Qualitätsmanagement sowie in den regulatorischen Anforderungen </li><li style="list-style-position:inside">Erfahrungen im Bereich Risk Management</li><li style="list-style-position:inside">Must have: Verhandlungssicher in Deutsch und Englisch </li><li style="list-style-position:inside">Eigenständige und zuverlässige Arbeitsweise </li></ul></div>
&nbsp;
Rahmendaten: Start: Juni/Juli 2023 Dauer: bis Ende des Jahres 2023 Auslastung: 4-5 Tage/Woche Einsatzort: remote &amp; on-site</div>

Project Manager MDR  (M/W/D)

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" dir="ltr" style="font-family:Arial; font-size:10pt">
<div>Expert Sales &amp; Production Controlling (M/W/D) 
&nbsp; 
Aufgaben:</div>

<div>&nbsp;</div>

<div>•&nbsp;&nbsp; &nbsp;Fachliche Verantwortung und Entwicklung eines Sales &amp; Produktionscontrolling Teams. 
•&nbsp;&nbsp; &nbsp;Entwickeln von Produktions-Controlling Verfahren zur Unterstützung der Business Units und Standardisierung der Berichterstattung. 
•&nbsp;&nbsp; &nbsp;Sicherstellung qualitativ hochwertiger Produktkostenkalkulationen für Planungs-, Forecast- und Abschlussprozesse 
•&nbsp;&nbsp; &nbsp;Bereitstellung von Daten und Analysen zu Produktionsprozessen und -kosten für die Entscheidungsfindung, Unterstützung der Business Partner auf lokaler und konsolidierter Ebene. 
•&nbsp;&nbsp; &nbsp;Sicherstellung des Key User Supports in relevanten Modulen (SAP CO-PA, ML, IBP, IP Sales/Cogs). 
•&nbsp;&nbsp; &nbsp;Mitarbeit in den Projekten "Sales-Controlling", "Transfer Pricing Policy" sowie bei der Unterstützung des S/4 Hana Roll-Outs</div>

<div>&nbsp;</div>

<div>Qualifikation:</div>

<div>&nbsp;</div>

<div>•&nbsp;&nbsp; &nbsp;Langjährige Erfahrung im Bereich Controlling eines international agierenden produzierenden Unternehmens 
•&nbsp;&nbsp; &nbsp;Fundierte Kenntnisse im Produktions-Controlling, sowie Erfahrung im Vertriebscontrolling wünschenswert 
•&nbsp;&nbsp; &nbsp;Einschlägige Erfahrung mit SAP R/3 sowie tiefgreifendes Verständnis der Module CO-PA, ML, IBP und ihrer Wechselwirkungen, Erfahrung mit S/4 HANA wünschenswert 
•&nbsp;&nbsp; &nbsp;Ausgezeichnete Anwenderkenntnisse in MS Office, v.a. MS Excel 
•&nbsp;&nbsp; &nbsp;Fließende Deutsch- und Englischkenntnisse (schriftlich und mündlich) 
&nbsp; 
Rahmendaten:</div>

<div>&nbsp; 
Start: ASAP 
Dauer: 12 Monate 
Auslastung: 5 Tage die Woche 
Einsatzort: Remote und vor Ort</div>
</div>

Senior Expert Sales & Production Controlling (M/W/D)

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" dir="ltr" style="font-family:Arial; font-size:10pt">
Interim HR Recruiter MedTech (M/W/D)

&nbsp;

Aufgaben:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Verantwortung für den kompletten Recruiting Prozess (Full Lifecycle Recruiting)</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Abstimmung mit den einzelnen Fachbereichen hinsichtlich Anforderungsprofilen</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Kandidatenscreening, sowie die Koordination und Führung von Interviews</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Active Sourcing über die entsprechenden Recruiting Kanäle</li>
</ul>

&nbsp;

Qualifikation:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Mehrjährige Erfahrung als (360 Grad) HR Recruiter</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Branchenerfahrung im Bereich Medizintechnik&nbsp;von großem Vorteil</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Solide Kenntnisse im Umgang mit Bewerbermanagementsystemen</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Deutsch und Englisch verhandlungssicher</li>
</ul>

&nbsp;

Rahmendaten:&nbsp;

Start: ASAP

Dauer: 3 Monate

Auslastung: 20-28 Std. / Woche (Mo-Do)

Einsatzort: Remote
</div>

Interim HR Recruiter MedTech (M/W/D)

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" dir="ltr" style="font-family:Arial; font-size:10pt">QA Auditor (M/F/D)
&nbsp;
Tasks:
&nbsp;
<ul style="margin-bottom:0cm; margin-top:0cm" type="disc"><li style="margin-left:8px;list-style-position:inside">Qualification audits in the in the EMEA region at plasma suppliers / service providers according to GxP and DIN ISO and evaluating the audit results,</li><li style="margin-left:8px;list-style-position:inside">Performance of risk analyses and evaluation of the impact on the qualification status of the plasma supplier / service provider; evaluation of corrective / preventive measures;</li><li style="margin-left:8px;list-style-position:inside">Review implementation and compliance with regulations and internal quality requirements for all facilities to be audited;</li><li style="margin-left:8px;list-style-position:inside">Help in further development of the established audit systems;</li><li style="margin-left:8px;list-style-position:inside">Creation and edition of standard operating procedures;</li><li style="margin-left:8px;list-style-position:inside">Updating various work lists to provide metrics up-to-date provision of key performance indicators;</li><li style="margin-left:8px;list-style-position:inside">Electronic acquisition and processing of non-conformance reports;</li><li style="margin-left:8px;list-style-position:inside">Participation in the implementation of trainings and workshops.</li></ul>
&nbsp;
Qualification:
&nbsp;
<ul style="margin-bottom:0cm; margin-top:0cm" type="disc"><li style="margin-left:8px;list-style-position:inside">Pharma and scientific Background</li><li style="margin-left:8px;list-style-position:inside">Solid professional experience as an auditor</li><li style="margin-left:8px;list-style-position:inside">German, English fluent – Nice to Have: French or Italian </li><li style="margin-left:8px;list-style-position:inside">Knowledge of quality management and GxP/DIN ISO area as well as audit/inspection experience</li><li style="margin-left:8px;list-style-position:inside">Willingness to travel </li></ul>
&nbsp;
Requirements:&nbsp;
Start: asap, latest Start: July 1rst 2023
Duration: 6 months or longer&nbsp;
Capacity: 4-5 days per week
Location: 100% remote but Onboarding Onsite 
&nbsp;</div>

QA Auditor

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" dir="ltr" style="font-family:Arial; font-size:10pt">
Clinical Safety Consultant (M/F/D)

&nbsp;

Tasks:

<ul>
	<li style="font-family: &quot;Open Sans&quot;, sans-serif; font-size: 15px; line-height: normal; margin: 0cm;">Aggregate reports (i.e. PSUR/DSURs): Lead project management role of PSUR/DSUR preparation for several marketed products in Europe overseeing a vendor. This includes planning, , process oversight, and document management in the system with input from each product safety physicians.</li>
	<li style="font-family: &quot;Open Sans&quot;, sans-serif; font-size: 15px; line-height: normal; margin: 0cm;">Risk Management (Signal identification, evaluation, mitigation): Consults with safety physician in updating key documents such as Risk Management Plans (EU-RMP), Signal Detection/Assessment Reports, and assessing new signals.</li>
	<li style="font-family: &quot;Open Sans&quot;, sans-serif; font-size: 15px; line-height: normal; margin: 0cm;">Safety Communication: Develops strategy for communicating safety information internally and externally (including EU Risk Minimisation Activities) with product safety physicians. May first author safety communications and take responsibilities of its implementation working with EU affiliates’ Local Safety Officers.</li>
	<li style="font-family: &quot;Open Sans&quot;, sans-serif; font-size: 15px; line-height: normal; margin: 0cm;">Project Management: Serves as a project manager for safety topics related to signal management and aggregate report and ensures adherence to project timeline.</li>
</ul>

&nbsp;

Qualification:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Bachelor’s degree at minimum required; Master or PhD with science background preferred.</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Possesses strong medical or pharmacovigilance knowledge min 5 years</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">5 years of project experience with an advanced degree; 7 years of project experience with a Bachelor’s degree</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Fluent business English (oral and written)</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Strong communication skill</li>
</ul>

&nbsp;

Requirements:&nbsp;&nbsp;

Start: Asap (latest 01.07.2023)

Duration: 12 months

Capacity: 30-40 hours per week

Location: 100% remote possible
</div>

Clinical Safety Consultant

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" dir="ltr" style="font-family:Arial; font-size:10pt">Einer unserer Kunden in München sucht aktuell freiberufliche Unterstützung als: SAP-Teilprojektleiter (M/W/D) Aufgaben:
<ul><li style="margin-left:8px;list-style-position:inside">Projektleitung einer SAP FI/CO Einführung </li><li style="margin-left:8px;list-style-position:inside">Definition des Scopes und Sicherstellung der Targets</li><li style="margin-left:8px;list-style-position:inside">Ganzheitliche Betreuung des FI-Anteils innerhalb des Projektes </li><li style="margin-left:8px;list-style-position:inside">Projektcontrolling </li><li style="margin-left:8px;list-style-position:inside">Koordination der Teams und Schnittstellenfunktion </li><li style="margin-left:8px;list-style-position:inside">Coaching und Schulung der Mitarbeiter </li></ul>
<div> Qualifikation:
<ul><li style="margin-left:8px;list-style-position:inside">Erfahrung in der Projektleitung </li><li style="margin-left:8px;list-style-position:inside">Erfahrung in der Implementierung von ERP-Systemen</li><li style="margin-left:8px;list-style-position:inside">Idealerweise tiefgründige User-Erfahrung aus dem&nbsp;Finance Umfeld&nbsp;</li><li style="margin-left:8px;list-style-position:inside">Deutsch und Englisch fließend</li></ul></div>
 Rahmendaten: Start: asap Dauer: 12 Monate Auslastung: 3-4 Tage/Woche Einsatzort: Remote/Onsite </div>

SAP-Teilprojektleiter

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" dir="ltr" style="font-family:Arial; font-size:10pt">Sales Manager Onkologie (M/W/D)
&nbsp;
Aufgaben:
<ul style="margin-bottom:0cm; margin-top:0cm" type="disc"><li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Beratung und Betreuung onkologischer&nbsp;Fachärzte&nbsp;(Kliniken und niedergelassene Ärzte)</li><li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Beratung bei der Analyse &amp; Erreichung von KPIs vor und nach der Markteinführung, einschließlich Umsatz- und Volumenziele</li><li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Mitgestaltung und Umsetzung der Vertriebsstrategie</li><li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Erstellung eines gebietsspezifischen Maßnahmenplanes, einschließlich Analyse, Segmentation </li><li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Durchführung von Seminaren, Verkaufspräsentationen, Produktdemonstrationen und Schulungen </li><li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Netzwerkpflege und Besuch von indikationsbezogenen Events </li><li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Enge Zusammenarbeit mit Marketing und Medical </li></ul>
&nbsp;
Qualifikation:
<ul style="margin-bottom:0cm; margin-top:0cm" type="disc"><li style="font-family: &quot;Open Sans&quot;, sans-serif; font-size: 15px; line-height: normal; margin: 0cm;">Mehrjährige Berufserfahrung im Außendienst, idealerweise im Pharma-Umfeld </li><li style="font-family: &quot;Open Sans&quot;, sans-serif; font-size: 15px; line-height: normal; margin: 0cm;">Projekterfahrung in der Gestaltung und Umsetzung von Verkaufsstrategien </li><li style="font-family: &quot;Open Sans&quot;, sans-serif; font-size: 15px; line-height: normal; margin: 0cm;">Umfassende Erfahrungen in der Onkologie/Specialty Care</li><li style="font-family: &quot;Open Sans&quot;, sans-serif; font-size: 15px; line-height: normal; margin: 0cm;">Verhandlungssichere Deutsch- und Englischkenntnisse </li></ul>
&nbsp;
Rahmendaten:&nbsp;
Start: 01.08.2023
Dauer: Mind. 12 Monate
Auslastung: 4-5 Tage die Woche
Einsatzort: remote &amp; Baden - Württemberg&nbsp;
&nbsp;
&nbsp;</div>

Sales Manager Onkologie

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" dir="ltr" style="font-family:Arial; font-size:10pt">
Prozess Spezialist Bioanalytik-Operations (M/W/D)

&nbsp;

Aufgaben:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="list-style-position:inside">Bearbeitung eingehender Probensendungen aus weltweiter Logistik im Hochdurchsatz, einschl. Eingang, Lagerung, Dokumentation und Problembehandlung</li>
	<li style="list-style-position:inside">Manuelle und automatisierte Probenverwaltung, samt Erfassung, Lagerung, Transport, Übergabe im Hochdurchsatz</li>
	<li style="list-style-position:inside">Verwaltung der Probendaten in komplexen Software-Systemen/Datenbanken (electronic laboratory notebook, Laboratory Information Management System) und Bearbeitung von Datensätzen (Tabellenkalkulation).</li>
	<li style="list-style-position:inside">SOP- und process-compliance und verantwortungsbewusster Umgang mit Patienten-/Probanden-Proben und Daten, samt transparenter Verarbeitung und Dokumentation von Vorfällen und Fehlern im Team</li>
	<li style="margin-bottom:13px;list-style-position:inside">Rigorose Dokumentation nach Good Laboratory Practice (GLP) und Good Clinical Practice</li>
</ul>

&nbsp;

Qualifikation:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="list-style-position:inside">Erfahrung im Bereich Proben - Bearbeitung&nbsp;</li>
	<li style="list-style-position:inside">Erfahrung in der Dokumentation nach GLP </li>
	<li style="list-style-position:inside">Sicher&nbsp;in Wort und Schrift (Deutsch und Englisch)</li>
	<li style="margin-bottom:13px;list-style-position:inside">Must have: sicherer Umgang mit LIMS und Microsoft Office </li>
</ul>

&nbsp;

Rahmendaten:&nbsp;

Start: Juni &amp; Juli 2023&nbsp;

Dauer: 12 Monate

Auslastung: 4-5 Tage die Woche

Einsatzort: Rheinland - Pfalz
</div>

Prozess Spezialist Bioanalytik-Operations

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" dir="ltr" style="font-family:Arial; font-size:10pt">
Design Engineer (M/W/D) 
&nbsp; 
Aufgaben:

<ul>
	<li style="margin-left:16px; margin-bottom:11px;list-style-position:inside">Design Verification, Validation and DHF (Design History File)</li>
	<li style="margin-left:16px; margin-bottom:11px;list-style-position:inside">Durchführung und Überwachung von CAPA-Maßnahmen</li>
	<li style="margin-left:16px; margin-bottom:11px;list-style-position:inside">Risikomanagement (Non-Comformity)</li>
	<li style="margin-left:16px; margin-bottom:11px;list-style-position:inside">Packaging and Testing von medizinischen Einwegartikeln und Kathetern</li>
	<li style="margin-left:16px; margin-bottom:11px;list-style-position:inside">Stakeholder Management</li>
</ul>

<div>&nbsp;Qualifikation:

<ul>
	<li style="margin-left:16px; margin-bottom:11px;list-style-position:inside">Erfahrungen in mechanischer Konstruktion, idealerweise Feinwerk- / bzw. Kunststofftechnik</li>
	<li style="margin-left:16px; margin-bottom:11px;list-style-position:inside">Branchenerfahrung in der Medizintechnik bzw. regulierten Industrie</li>
	<li style="margin-left:16px; margin-bottom:11px;list-style-position:inside">Kenntnisse mit der CAD-Software SolidWorks (nice to have)</li>
	<li style="margin-left:16px; margin-bottom:11px;list-style-position:inside">Eigenständige Arbeitsweise, Hands-On Mentalität und Teamplayer</li>
</ul>
</div>

Rahmendaten:&nbsp; 
Start: ASAP 
Dauer: 3 Monate (Verlängerung möglich) 
Auslastung: 5 Tage / Woche 
Einsatzort: Dresden und Remote
</div>

Design Engineer (m/w/d)

<div data-wrapper="true" dir="ltr" style="font-family:Arial; font-size:10pt">
Entwicklungsingenieur (M/W/D)

&nbsp;

Aufgaben:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="list-style-position:inside;margin-left:0cm;">Planung, Konstruktion und Umsetzung von medizinischen Einwegartikeln (Kathetern)</li>
	<li style="list-style-position:inside;margin-left:0cm;">Projekt- und Schnittstellenmanagement</li>
	<li style="list-style-position:inside;margin-left:0cm;">Enge Zusammenarbeit mit CAD-Konstruktion</li>
	<li style="list-style-position:inside;margin-left:0cm;">Koordination der Materialbestellungen</li>
	<li style="list-style-position:inside;margin-left:0cm;">Dokumentenmanagement</li>
</ul>

&nbsp;

Qualifikation:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="margin-left:8px;list-style-position:inside">Erfahrungen in mechanischer Konstruktion, idealerweise Feinwerk- / bzw. Kunststofftechnik</li>
	<li style="margin-left:8px;list-style-position:inside">Branchenerfahrung in der Medizintechnik bzw. regulierten Industrie</li>
	<li style="margin-left:8px;list-style-position:inside">Kenntnisse mit der CAD-Software SolidWorks (nice to have)</li>
	<li style="margin-left:8px;list-style-position:inside">Eigenständige Arbeitsweise, Hands-On Mentalität und Teamplayer</li>
</ul>

&nbsp;

Rahmendaten:&nbsp;

Start: ASAP

Dauer: 3 Monate (Verlängerung möglich)

Auslastung: 5 Tage / Woche

Einsatzort: Dresden und Remote
</div>

Entwicklungsingenieur (m/w/d)

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" dir="ltr" style="font-family:Arial; font-size:10pt">
Consultant Biochemistry (M/F/D)

&nbsp;

Tasks:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Review the existing hypothesis regarding the oxidation of Tween and its potential impact on MPO enzyme activity</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Provide in-depth knowledge and expertise in the chemistry of Tween oxidation and its reaction mechanisms</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Evaluate the potential impact of Tween oxidation on the performance and characteristics of immunoassays, specifically focusing on the detection and quantification of MPO or related analytes.</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Propose analytical tools, techniques, and assays to assess the effect of Tween oxidation on immunoassay performance</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Develop experimental protocols to validate the hypothesis, including appropriate positive and negative controls</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Analyze the experimental data collected from the assays and analytical tools to evaluate the impact of Tween oxidation on the performance and reliability of immunoassays.</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Interpret the results and draw meaningful conclusions to support or reject the initial hypothesis</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Provide clear and actionable recommendations based on the research outcomes, suggesting potential mitigation strategies or areas for further investigation</li>
</ul>

&nbsp;

Qualification:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">A strong background in chemistry, preferably with expertise in oxidation mechanisms and enzymology</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Extensive experience in immunoassay development, particularly related to antibody-antigen interactions and assay performance</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Familiarity with Tween 20 and its role as a stabilizer in biotherapeutic products and immunoassays</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Proficiency in designing and executing analytical experiments, including experience with relevant analytical tools and assays</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Excellent analytical and problem-solving skills, with the ability to interpret complex data and draw meaningful conclusions</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Strong communication skills, both written and verbal, to effectively communicate research findings and recommendations to stakeholders</li>
</ul>

&nbsp;

Requirements:&nbsp;

Start: asap, latest 6/15

Duration: 1 month +

Capacity: 2-3 days per week

Location: California, but mostly Remote

&nbsp;
</div>

Consultant Biochemistry

<div data-wrapper="true" dir="ltr" style="font-family:Arial; font-size:10pt">
Project Lead MDR (M/F/D)

&nbsp;

Tasks:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Lead all relevant tasks related to an EU submission of an existing product</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Ensure Project Management incl. Budget Planning, Milestone Planning on time</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Cross-functional work with R&amp;D, Quality, Regulatory and Marketing</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Drive Project toward&nbsp;MDR Readiness</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Optimization of Project structures</li>
</ul>

&nbsp;

Qualification:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Degree in Engineering or similar</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Robust Project Lead experience within regulated industries, preferably MedTech</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Vast knowledge about EU submissions, MDR</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Strong communication, people and organization skills</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Nice to have: Experience within Microsurgery</li>
</ul>

&nbsp;

Requirements:&nbsp;

Start: 01/06/23

Duration: 6 months +

Capacity: 3-5 days per week

Location: Onsite in Missouri &amp; Remote

&nbsp;
</div>

Project Lead MDR

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" dir="ltr" style="font-family:Arial; font-size:10pt">
Senior Quality Assurance Expert (M/W/D) 
 
Tasks:

<ul>
	<li style="margin-bottom:11px;list-style-position:inside">Define QA strategy and execution in development projects</li>
	<li style="margin-bottom:11px;list-style-position:inside">Consult&nbsp;the QA team with expertise&nbsp;</li>
	<li style="margin-bottom:11px;list-style-position:inside">Ensure adherence to QA principles and best practices</li>
	<li style="margin-bottom:11px;list-style-position:inside">Provide regular updates to senior leadership on compliance and risks</li>
	<li style="margin-bottom:11px;list-style-position:inside">Implement and enhance the Quality Management System (QMS)</li>
	<li style="margin-bottom:11px;list-style-position:inside">Maintain GMP, GLP, and GCP compliance for manufacturing and trials</li>
	<li style="margin-bottom:11px;list-style-position:inside">Drive continuous improvement and foster excellence</li>
	<li style="margin-bottom:11px;list-style-position:inside">Oversee supplier quality, inspections, regulatory filings&nbsp;and validation activities</li>
</ul>

<div> 
 
Qualification:

<ul>
	<li style="margin-bottom:11px;list-style-position:inside">Bachelor's degree in science or related field with post-graduate studies</li>
	<li style="margin-bottom:11px;list-style-position:inside">Minimum 10 years of experience in biopharmaceutical quality assurance</li>
	<li style="margin-bottom:11px;list-style-position:inside">Proven track record in developing and improving systems for GxP compliance</li>
	<li style="margin-bottom:11px;list-style-position:inside">Strong understanding and application of quality principles and industry standards</li>
	<li style="margin-bottom:11px;list-style-position:inside">Knowledge of GMP, GLP, and GCP regulations, with expertise in sterility manufacturing for pharmaceutical products</li>
	<li style="margin-bottom:11px;list-style-position:inside">Business English must have</li>
</ul>
</div>

 
 
Frame Data: 
Start: 01.06.2023 
Duration: 6 Months 
FTE: Fulltime 
Einsatzort: remote &amp; onsite (2 days a week / every 2 weeks for 4 days)

&nbsp;
</div>

Senior Quality Assurance Expert

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Interim-Galenik-Experte (M/W/D)

&nbsp;

Aufgaben:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Formulierungsentwicklung in verschiedenen Darreichungsformen</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Auswertung, Verfassung &amp; Prüfen von Entwicklungsberichten</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Troubleshooting von pharm. Herstellungsprozessen und Formulierungen</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Experimentelle Arbeit zur Herstellung und Prüfung von Arzneimitteln</li>
</ul>

&nbsp;

Qualifikation:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Studium der Pharmazie, Biotechnologie oder vergleichbar</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Kenntnisse der pharmazeutischen Entwicklung und Herstellung versch. Darreichungsformen</li>
</ul>

&nbsp;

Rahmendaten:&nbsp;

Start: ab sofort, spät. Mai/Juni

Dauer: 6-12 Monate

Auslastung: 3-5 Tage die Woche

Einsatzort: Großraum München &amp; remote
</div>

Interim Galenik-Experte

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
CMC Project Manager Biologics (M/F/D)

&nbsp;

Tasks:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Manage project timelines, budget, and resources to ensure successful project delivery</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Work closely with cross-functional teams, internally and externally (large CMO), to ensure timely delivery of project milestones</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Develop and implement CMC regulatory strategies to ensure compliance with regulatory requirements and guidelines</li>
	<li style="font-family:&quot;Open Sans&quot;;font-size:12.0pt;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Ensure all activities related to CMC are in accordance with GMP, GLP, and other regulatory requirements</li>
	<li style="font-family:&quot;Open Sans&quot;;font-size:12.0pt;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Advise on BLA Submission Strategy</li>
</ul>

&nbsp;

Qualification:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="font-family:&quot;Open Sans&quot;;font-size:12.0pt;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Degree in a scientific or engineering discipline, such as chemistry, biology, chemical engineering, or related fields</li>
	<li style="font-family:&quot;Open Sans&quot;;font-size:12.0pt;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Knowledge of regulatory requirements and guidelines related to CMC activities for biologics products</li>
	<li style="font-family:&quot;Open Sans&quot;;font-size:12.0pt;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Experience with biologics process development&nbsp;and scale-up activities</li>
	<li style="font-family:&quot;Open Sans&quot;;font-size:12.0pt;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Successful track record with BLA Submissions, Hands-On Approach</li>
	<li style="font-family:&quot;Open Sans&quot;;font-size:12.0pt;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Excellent communication, leadership, and collaboration skills, also culturally</li>
	<li style="font-family:&quot;Open Sans&quot;;font-size:12.0pt;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Ability to manage multiple priorities and projects simultaneously in a dynamic environment</li>
</ul>

&nbsp;

Requirements:&nbsp;

Start: 4/15/23, latest 5/15/23

Duration: 18 months

Capacity: 3 days per week

Location: Remote

&nbsp;
</div>

CMC Project Manager Biologics

<div data-wrapper="true" style="font-size:10pt;font-family:Arial;">Business Development Executive (M/F/D)
&nbsp;
Tasks:
<ul style="margin-bottom:0cm; margin-top:0cm" type="disc"><li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Identifying and In-licensing IP</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Commercialization of client's product with industry-sponsored trials</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Establishment of the product&nbsp;with hospitals </li></ul>
&nbsp;
Qualification:
<ul style="margin-bottom:0cm; margin-top:0cm" type="disc"><li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Track Record in BD within Life Sciences, Cancer Treatment</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">ideally, experience with Precision Medicine</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Network within the US in the field of Oncology</li></ul>
&nbsp;
Requirements:&nbsp;
Start: asap, latest Mid April
Duration: 6 months
Capacity: approx. 10 hours / month
Location: Remote
&nbsp;</div>

Business Development Executive

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Executive Biologist (M/F/D)

&nbsp;

Tasks:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Advise on general company road mapping, Strategy (Startup)</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">IP Development</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Advise on Research Activities</li>
</ul>

&nbsp;

Qualification:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Degree in Biology or Biomedical Engineering</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Industry Experience within Organoids</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Experience with Cancer Biology Research, ideally organoid lab background</li>
</ul>

&nbsp;

Requirements:&nbsp;

Start: asap

Duration: 6 months

Capacity: approx. 10 hours / month

Location: Remote

&nbsp;
</div>

Executive Biologist

<div data-wrapper="true" style="font-size:10pt;font-family:Arial;">Oncology Advisor (M/F/D)

&nbsp;

Tasks:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Guidance on indications for the client's products</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Advisory on clinical trial design</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Sparring on Oncology Research Topics</li>
</ul>

&nbsp;

Qualification:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Oncologist</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Specialty:&nbsp;gynecologic oncology or&nbsp;cancer surgeon</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Experience with clinical trials in Europe (design and lead)</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Detail-oriented, systematic-analytical, driven</li>
</ul>

&nbsp;

Requirements:&nbsp;

Start: asap, latest Mid April

Duration: 6 months

Capacity: approx. 10 hours / month

Location: Fully Remote

&nbsp;</div>

Oncology Advisor

<div data-wrapper="true" style="font-family:Arial; font-size:10pt">
<span style="font-family:-apple-system,BlinkMacSystemFont,&quot;Segoe UI&quot;,system-ui,&quot;Apple Color Emoji&quot;,&quot;Segoe UI Emoji&quot;,&quot;Segoe UI Web&quot;,sans-serif; font-size:14px; white-space:pre-wrap">Einer unserer Pharma-Kunden in Deutschland sucht aktuell freiberufliche Unterstützung als: 
 
Market Access Manager (M/W/D) 
 
Aufgaben:

<div>&nbsp;
<ul>
	<li><span style="font-family:-apple-system,BlinkMacSystemFont,&quot;Segoe UI&quot;,system-ui,&quot;Apple Color Emoji&quot;,&quot;Segoe UI Emoji&quot;,&quot;Segoe UI Web&quot;,sans-serif; font-size:14px; white-space:pre-wrap">Unterstützung im nationalen und regionalen Market Access</li>
	<li><span style="font-family:-apple-system,BlinkMacSystemFont,&quot;Segoe UI&quot;,system-ui,&quot;Apple Color Emoji&quot;,&quot;Segoe UI Emoji&quot;,&quot;Segoe UI Web&quot;,sans-serif; font-size:14px; white-space:pre-wrap">Unterstützung bei der Erarbeitung einer Value Story&nbsp;</li>
	<li><span style="font-family:-apple-system,BlinkMacSystemFont,&quot;Segoe UI&quot;,system-ui,&quot;Apple Color Emoji&quot;,&quot;Segoe UI Emoji&quot;,&quot;Segoe UI Web&quot;,sans-serif; font-size:14px; white-space:pre-wrap">Unterstützung der Preisverhandlung, Analyse und Erstellung Unterlagen</li>
	<li><span style="font-family:-apple-system,BlinkMacSystemFont,&quot;Segoe UI&quot;,system-ui,&quot;Apple Color Emoji&quot;,&quot;Segoe UI Emoji&quot;,&quot;Segoe UI Web&quot;,sans-serif; font-size:14px; white-space:pre-wrap">Vorbereitung von Meetings &amp; Präsentationen mit dem G-BA</li>
	<li><span style="font-family:-apple-system,BlinkMacSystemFont,&quot;Segoe UI&quot;,system-ui,&quot;Apple Color Emoji&quot;,&quot;Segoe UI Emoji&quot;,&quot;Segoe UI Web&quot;,sans-serif; font-size:14px; white-space:pre-wrap">Unterstützung bei Themen zu Value Based Solution</li>
	<li><span style="font-family:-apple-system,BlinkMacSystemFont,&quot;Segoe UI&quot;,system-ui,&quot;Apple Color Emoji&quot;,&quot;Segoe UI Emoji&quot;,&quot;Segoe UI Web&quot;,sans-serif; font-size:14px; white-space:pre-wrap">Preis Recherche</li>
</ul>

 
<span style="font-family:-apple-system,BlinkMacSystemFont,&quot;Segoe UI&quot;,system-ui,&quot;Apple Color Emoji&quot;,&quot;Segoe UI Emoji&quot;,&quot;Segoe UI Web&quot;,sans-serif; font-size:14px; white-space:pre-wrap">Qualifikation:

<ul>
	<li><span style="font-family:-apple-system,BlinkMacSystemFont,&quot;Segoe UI&quot;,system-ui,&quot;Apple Color Emoji&quot;,&quot;Segoe UI Emoji&quot;,&quot;Segoe UI Web&quot;,sans-serif; font-size:14px; white-space:pre-wrap">Erfahrung im Bereich Market Access, AMNOG, G-BA</li>
	<li><span style="font-family:-apple-system,BlinkMacSystemFont,&quot;Segoe UI&quot;,system-ui,&quot;Apple Color Emoji&quot;,&quot;Segoe UI Emoji&quot;,&quot;Segoe UI Web&quot;,sans-serif; font-size:14px; white-space:pre-wrap">Kenntnisse der aktuellen gesundheitspolitischen Entwicklungen in Deutschland</li>
	<li><span style="font-family:-apple-system,BlinkMacSystemFont,&quot;Segoe UI&quot;,system-ui,&quot;Apple Color Emoji&quot;,&quot;Segoe UI Emoji&quot;,&quot;Segoe UI Web&quot;,sans-serif; font-size:14px; white-space:pre-wrap">Erfahrung in der Onkologie wünschenswert</li>
	<li><span style="font-family:-apple-system,BlinkMacSystemFont,&quot;Segoe UI&quot;,system-ui,&quot;Apple Color Emoji&quot;,&quot;Segoe UI Emoji&quot;,&quot;Segoe UI Web&quot;,sans-serif; font-size:14px; white-space:pre-wrap">Fließende Deutsch- und Englisch-Kenntnisse</li>
</ul>

 
<span style="font-family:-apple-system,BlinkMacSystemFont,&quot;Segoe UI&quot;,system-ui,&quot;Apple Color Emoji&quot;,&quot;Segoe UI Emoji&quot;,&quot;Segoe UI Web&quot;,sans-serif; font-size:14px; white-space:pre-wrap">Rahmendaten:

<ul>
	<li><span style="font-family:-apple-system,BlinkMacSystemFont,&quot;Segoe UI&quot;,system-ui,&quot;Apple Color Emoji&quot;,&quot;Segoe UI Emoji&quot;,&quot;Segoe UI Web&quot;,sans-serif; font-size:14px; white-space:pre-wrap">Start: April / Mai 2023&nbsp;</li>
	<li><span style="font-family:-apple-system,BlinkMacSystemFont,&quot;Segoe UI&quot;,system-ui,&quot;Apple Color Emoji&quot;,&quot;Segoe UI Emoji&quot;,&quot;Segoe UI Web&quot;,sans-serif; font-size:14px; white-space:pre-wrap">Dauer: 6 Monate, Option auf eine Verlängerung&nbsp;</li>
	<li><span style="font-family:-apple-system,BlinkMacSystemFont,&quot;Segoe UI&quot;,system-ui,&quot;Apple Color Emoji&quot;,&quot;Segoe UI Emoji&quot;,&quot;Segoe UI Web&quot;,sans-serif; font-size:14px; white-space:pre-wrap">Auslastung: ab 3 Tage/ Woche, remote</li>
</ul>
 
 
&nbsp;</div>

&nbsp;
</div>

Market Access Manager

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Construction Manager (M/F/D)

&nbsp;

Tasks:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li class="Bullet1" style="margin-right:30px; margin-top:4px; margin-bottom:4px;list-style-position:inside">Coordinate and control the service providers and suppliers, the individual work steps as well as the material flows.</li>
	<li style="list-style-position:inside">Manage all owned works and coordinate them with the assigned EPCM company – including Mechanical, Electrical, Ductwork </li>
	<li style="list-style-position:inside">Lead external planning teams and construction companies assigned where not scope of EPCM. </li>
	<li class="Bullet1" style="margin-right:30px; margin-top:4px; margin-bottom:4px;list-style-position:inside">Ensure smooth flow of construction work, site organization and take care of construction site facilities together with EPCM company. </li>
	<li class="Bullet1" style="margin-right:30px; margin-top:4px; margin-bottom:4px;list-style-position:inside">Ensure structural realization according to the planning specifications as well as according to the applicable regulations and building standards.</li>
	<li style="list-style-position:inside">Coordination with other Construction Managers to ensure activities planned are fully reviewed for impact with other ongoing projects.</li>
	<li style="list-style-position:inside">Technical and commercial negotiations with suppliers</li>
	<li class="Bullet1" style="margin-right:30px; margin-top:4px; margin-bottom:4px;list-style-position:inside">Equipment coordination with suppliers, EPCM team and external Logistics team to ensure sizing, crate configuration and entry method to site are all reviewed and approved prior to equipment installation </li>
	<li class="Bullet1" style="margin-right:30px; margin-top:4px; margin-bottom:4px;list-style-position:inside">Continuous improvement of Construction Management Plan and Construction Health and Safety Plan with the EPCM </li>
	<li class="Bullet1" style="margin-right:30px; margin-top:4px; margin-bottom:4px;list-style-position:inside">Generation of Weekly reports and lookaheads on works to be completed in conjunction with the EPCM</li>
	<li style="list-style-position:inside">Ensure that the project objectives cost, deadlines, quality and safety of the assigned construction projects are achieved</li>
	<li class="Bullet1" style="margin-right:30px; margin-top:4px; margin-bottom:4px;list-style-position:inside">Maintain a working knowledge of all organisational installation and construction procedures and standards to enable site reviews against them on an ongoing basis throughout the project </li>
	<li class="Bullet1" style="margin-right:30px; margin-top:4px; margin-bottom:4px;list-style-position:inside">Maintain an expert view on the 3D Coordination Building Information Model (BIM) so all clashes can be resolved and the installation checked against the model on an ongoing basis</li>
	<li class="Bullet1" style="margin-right:30px; margin-top:4px; margin-bottom:4px;list-style-position:inside">Checking the quality of materials as well as the technical, constructional and design quality in the execution.&nbsp; </li>
	<li class="Bullet1" style="margin-right:30px; margin-top:4px; margin-bottom:4px;list-style-position:inside">Ongoing quality checks of mechanical pipework, pipework supports, cable trays and ductworks in compliance with the approved 3D Model and all standards and close-out any issues found with EPCM company.</li>
	<li class="Bullet1" style="margin-right:30px; margin-top:4px; margin-bottom:4px;list-style-position:inside">Support all construction testing as a `witness` and ensure all test documentation is completed and closed (pressure testing of pipework etc)</li>
	<li class="Bullet1" style="margin-right:30px; margin-top:4px; margin-bottom:4px;list-style-position:inside">Review all Contractor Turnover Documentation for accuracy against the approved design and resolve punches with the individual contractors.</li>
	<li class="Bullet1" style="margin-right:30px; margin-top:4px; margin-bottom:4px;list-style-position:inside">System walkdowns to achieve Mechanical completion and drive punch list to closure with EPCM and individual contractor companies</li>
	<li class="Bullet1" style="margin-right:30px; margin-top:4px; margin-bottom:4px;list-style-position:inside">Safety culture to be implemented on project to ensure Zero Lost Time Incidents – work with EPCM Safety Team to implement initiatives, standards, processes to achieve this</li>
	<li class="Bullet1" style="margin-right:30px; margin-top:4px; margin-bottom:4px;list-style-position:inside">Coordinate safety reviews on an ongoing basis independently, with internal EHS and also with the EPCM EHS Team to ensure safety is being proactively reviewed and managed</li>
	<li class="Bullet1" style="margin-right:30px; margin-top:4px; margin-bottom:4px;list-style-position:inside">Ensure safety observations are identified, corrective actions put in place and closed out and communicated to all contractors on the project</li>
</ul>

&nbsp;

Qualification:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li class="Bullet1" style="margin-top:4px; margin-bottom:4px;list-style-position:inside">Bachelor or Master’s degree in Civil Engineering, Architecture or other relevant engineering discipline</li>
	<li class="Bullet1" style="margin-top:4px; margin-bottom:4px;list-style-position:inside">A minimum of 10 years’ experience in a similar role</li>
	<li class="Bullet1" style="margin-top:4px; margin-bottom:4px;list-style-position:inside">Experience in managing large industrial construction projects</li>
	<li class="Bullet1" style="margin-top:4px; margin-bottom:4px;list-style-position:inside">Experience in managing pharmaceutical construction projects - including cleanroom construction up to GMP grade C (ISO 8)</li>
	<li class="Bullet1" style="margin-top:4px; margin-bottom:4px;list-style-position:inside">Knowledge and experience of (BIM)</li>
	<li class="Bullet1" style="margin-top:4px; margin-bottom:4px;list-style-position:inside">Knowledge and experience of project scheduling using Primavera P6 or MS Project</li>
	<li class="Bullet1" style="margin-top:4px; margin-bottom:4px;list-style-position:inside">Knowledge of clean and black utility requirements for the biopharmaceutical industry</li>
	<li class="Bullet1" style="margin-top:4px; margin-bottom:4px;list-style-position:inside">Structured thinking, problem solving with open and excellent communication skills (spoken and written)</li>
	<li class="Bullet1" style="margin-top:4px; margin-bottom:4px;list-style-position:inside">Ability to work in a multidisciplinary team</li>
	<li class="Bullet1" style="margin-top:4px; margin-bottom:4px;list-style-position:inside">Excellent German and English language ability </li>
</ul>

&nbsp;

Requirements:&nbsp;

Start: March / April 2023

Duration: 12 months

Capacity: 5 days per week

Location: Visp, Switzerland

&nbsp;
</div>

Construction Manager

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Senior CRA (M/F/D)

&nbsp;

Tasks:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Manage clinical study - Phase 1</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Monitoring activities, such as review of study protocols</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Clinical Project Management</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Manage Central Labs&nbsp;</li>
</ul>

&nbsp;

Qualification:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Profound experience as Senior CRA, Clinical Project Manager, Clinical Monitoring</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Experience with Phase 1 Studies</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Keen in writing and reviewing clinical protocols</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Nice to have: Experience within Oncology</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Detail-oriented, precise, high-quality standards</li>
</ul>

&nbsp;

Requirements:&nbsp;

Start: asap, latest beginning of 2023

Duration: 12-18 months

Capacity: 3-4 days per week

Location: California, but 100% Remote

&nbsp;
</div>

Senior CRA

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
CAD-Konstrukteur (M/W/D)

 
Aufgaben:

<ul>
	<li style="margin-bottom:11px;list-style-position:inside">Annahme von Aufträgen für Sonderteilen, Klärung von Auftragsdetails mit Kunden und techn. Innendienst</li>
	<li style="margin-bottom:11px;list-style-position:inside">Erstellen von CAD-Zeichnungen (SolidWorks)</li>
	<li style="margin-bottom:11px;list-style-position:inside">Erteilen des Auftrages an unsere Lieferanten im In- und Ausland und der Dienstleister, Überwachung des Auftrages, Prüfen bei Fertigstellung</li>
	<li style="margin-bottom:11px;list-style-position:inside">Verwaltung von Teilen (Ein- und Ausbuchung der Teile im ERP)</li>
	<li style="margin-bottom:11px;list-style-position:inside">Koordination mit der Werkstatt sowie Machbarkeitsprüfung</li>
	<li style="margin-bottom:11px;list-style-position:inside">Sicherung und Einhaltung der Abbauprozesse und des QM</li>
	<li style="margin-bottom:11px;list-style-position:inside">Suche nach Ersatzlieferanten und Ersatzdienstleistern</li>
	<li style="margin-bottom:11px;list-style-position:inside">Vorschau und Lagerbestandssicherung von Teilen und Fertigprodukten</li>
	<li style="margin-bottom:11px;list-style-position:inside">Mitwirkung bei der Entwicklung neuer Produkte</li>
</ul>

<div>Qualifikation: 
&nbsp;
<ul>
	<li style="list-style-position:inside">Qualifikation als Konstrukteur / Techniker / Verfahrenstechniker</li>
	<li style="list-style-position:inside">Erfahrungen im Behälterbau / Anlagenbau / Rohrleitungsbau im Bereich Life Science (zwingend erforderlich)</li>
	<li style="list-style-position:inside">Fliessend Deutsch und Grundkenntnisse in Englisch</li>
</ul>
</div>

&nbsp; 
Rahmendaten:&nbsp; 
Start: ab sofort 
Dauer: 12 Monate (+Übernahme) 
Auslastung: 5 Tage die Woche vor Ort 
Einsatzort: nähe Zürich 
&nbsp; 
&nbsp;
</div>

CAD-Konstrukteur

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Einer unserer Kunden aus dem Bereich Biotech/Medical Device in Deutschland sucht derzeit freiberufliche Unterstützung als:

Sales Agent Germany Surgery (D/M/W) 
Regionen: Nord-Ost&nbsp; 
 
 
Aufgaben:

<ul>
	<li style="list-style-position: inside;">Aktive und enthusiastische Entwicklung des deutschen Marktes</li>
	<li style="list-style-position: inside;">Erreichen von Vertriebszielen</li>
	<li style="list-style-position: inside;">Betreuung aktiver und potenzieller Kunden auf produkt- und prozessualer / administrativer Ebene</li>
	<li style="list-style-position: inside;">Identifizierung von Wachstumschancen</li>
	<li style="list-style-position: inside;">Kontinuierliches Reporting und Auswertung der Ergebnisse</li>
</ul>

Qualifikation:

<ul>
	<li style="list-style-position: inside;">Qualifizierung als "Pharmareferent</li>
	<li style="list-style-position: inside;">Hohe Affinität/Begeisterung für die Vermarktung hochwissenschaftlicher und technologisch fortschrittlicher medizinischer Produkte</li>
	<li style="list-style-position: inside;">Fähigkeit zu Gesprächen auf Augenhöhe mit Chirurgen (Hand, Trauma, Orthopädie) Verkaufserfahrung</li>
	<li style="list-style-position: inside;">Gutes Verständnis von Operationssälen und der Arbeitsumgebung von Chirurgen</li>
	<li style="list-style-position: inside;">Fähigkeit, komplexe klinische Studien zu verstehen und als Verkaufsinstrument zu nutzen</li>
	<li style="list-style-position: inside;">Fließende Beherrschung der deutschen und englischen Sprache</li>
	<li style="list-style-position: inside;">Bereitschaft zu Reisen nach Bedarf</li>
	<li style="list-style-position: inside;">Verständnis NUB Verfahren / Einzelfallantrag ist von Vorteil</li>
</ul>

Anforderungen: 
Beginn: Januar/Februar 2023 
Dauer: 6 Monate+ 
Kapazität: tbd
</div>

Sales Agent Surgery

<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">
<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>