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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 contractor pool. This will give me the opportunity to receive further exciting offers. By being included in the contractor 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" style="font-size:10pt;font-family:Arial;">Pharma Compliance Consultant (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;">Consulting on all HCP relevant compliance matters (e.g. promotions)</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;">Consulting on the execution of contracts regarding sponsorships</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;">Responsible for all Western countries, especially France, UK, Italy&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;">Cross-functional collaboration</li>
</ul>

&nbsp;

Qualification:

<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;">Laywer between junior and mid-level seniority</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Relevant experience with Pharma Compliance topics on a European level</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Experience working on international matters / matters in multiple countries</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Business fluency in English, additional languages are an asset</li>
</ul>

&nbsp;

Requirements:&nbsp;

Start: Latest 02/2023

Duration: until end of August 2023

Capacity: from 3 days per week

Location: remote

&nbsp;</div>

Legal & Compliance Consultant

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

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;">Responsible&nbsp;for planning, monitoring and controlling of campaigns based on KPIs, benchmarks and insights</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;">Responsibile&nbsp;for the implementation of CANVAS and agency onboarding</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;">Advising the brand teams with regard to channels and platforms that are available and can be used nationwide Product brand-specific cross-media national and international campaigns</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;">Broad experience in the application of cross-media communication tools (with a focus on digital media)&nbsp;&nbsp;</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;">Exprience in the pharmaceutical industy with prescription products, ideally in the area of rare diseases</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 German and very good English skills</li>
</ul>

&nbsp;

Requirements:&nbsp;

Start: 01.01.2023

Duration: 6-12 months

Capacity: 5 days per week

Location: Remote
</div>

Digital Marketing Manager

<div data-wrapper="true" style="font-size:10pt;font-family:Arial;">Regulatory Affairs Manager (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;">Gap-Analyse der aktuelle Quality/CMC</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Vorbereiten, Verfassen und review der NDA-Zulassungsdokumente</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Überprüfung/Vorbereitung von Zulassungsdokumente</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Beratung zur Erstellung des Briefingsbooks für die FDA</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Abstimmung mit allen relevanten Steakholdern</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;">Langjährige Erfahrung im regulatorischen Umfeld (im Besonderen mit der FDA)</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Verhandlungsicher in Englisch (Wort und Schrift)</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Strategisches Wissen in Kombination mit einer lösungsorientierten Arbeitsweise&nbsp;</li>
</ul>

&nbsp;

Rahmendaten:&nbsp;

Start: asap

Dauer: 3 Monate

Auslastung: 2 Tage die Woche

Einsatzort: remote

&nbsp;</div>

Regulatory Affairs Manager

<div data-wrapper="true" style="font-size:10pt;font-family:Arial;">SAP Application Manager SD/WM (M/F/D)

&nbsp;

Tasks:

<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;&nbsp; &nbsp;Analyzes and defines solutions within the Incident, Change-, Project-Process 
•&nbsp;&nbsp; &nbsp;Understands the business issues, needs, and challenges 
•&nbsp;&nbsp; &nbsp;Suggests areas of improvement 
•&nbsp;&nbsp; &nbsp;Leads projects and initiatives in the SD and WM area 
•&nbsp;&nbsp; &nbsp;Reviews and edits requirements, specifications, business processes, and recommendations related to the proposed solution 
•&nbsp;&nbsp; &nbsp;Develop functional specifications and system design specifications 
•&nbsp;&nbsp; &nbsp;Recommends technical solutions 
•&nbsp;&nbsp; &nbsp;Cooperating with consultants from other modules, such as PP and MM&nbsp; 
•&nbsp;&nbsp; &nbsp;Contributes to driving Biotronik into Digitalization 
•&nbsp;&nbsp; &nbsp;Drive for process harmonization and prepare for a future S4 transformation project</div>

&nbsp;

Qualification:

<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;&nbsp; &nbsp;Very good understanding of SAP SD and related modules like MM or PP 
•&nbsp;&nbsp; &nbsp;Bachelor in applied computer science, Information Technology, or similar 
•&nbsp;&nbsp; &nbsp;More than five years of experience in the area of SAP SD and/or SAP WM&nbsp; 
•&nbsp;&nbsp; &nbsp;Professional experience in projects and rollouts 
•&nbsp;&nbsp; &nbsp;Excellent language skills in English. C-Level German is a plus</div>

&nbsp;

Requirements:&nbsp;

Start: February 2023

Duration: 3-9 months

Capacity: 4-5 days per week

Location: remote

&nbsp;</div>

SAP Application Manager SD/WM

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

<ul>
	<li style="font-family: &quot;Open Sans&quot;, sans-serif; font-size: 15px; line-height: normal; margin: 0cm;">Projekt- und Beratungsleistung bei der Vorbereitung des Jahresabschlusses (HGB)</li>
	<li style="font-family:&quot;Arial&quot;,sans-serif;font-size:11pt;line-height:normal;margin:0cm;">Beratungsleistung bei Kreditoren- &amp; Debitorenbuchungen / Asset Management</li>
	<li style="font-family:&quot;Arial&quot;,sans-serif;font-size:11pt;line-height:normal;margin:0cm;">Beratende Unterstützung bei UmSt. Voranmeldungen / bzw. ZM-Meldungen</li>
	<li style="font-family:&quot;Arial&quot;,sans-serif;font-size:11pt;line-height:normal;margin:0cm;">Beratungsleistung bei den geplanten Kontenabstimmungen / Abschlussbuchungen</li>
	<li style="font-family:&quot;Arial&quot;,sans-serif;font-size:11pt;line-height:normal;margin:0cm;">Kommunikation mit den Schnittstellenabteilungen und Steuerkanzlei</li>
</ul>

<div>&nbsp;&nbsp;Qualifikation:

<ul>
	<li style="font-family:&quot;Arial&quot;,sans-serif;font-size:11pt;line-height:normal;margin:0cm;">Fundierte Erfahrung in der Buchhaltung sowie Jahresabschlusstätigkeiten nach HGB</li>
	<li style="font-family:&quot;Arial&quot;,sans-serif;font-size:11pt;line-height:normal;margin:0cm;">Gute allgemeine ERP-Erfahrungen oder Kenntnisse in Pro Alpha wünschenswert&nbsp;</li>
	<li style="font-family:&quot;Arial&quot;,sans-serif;font-size:11pt;line-height:normal;margin:0cm;">Deutsch verhandlungssicher sowie gute schriftliche Englischkenntnisse</li>
	<li style="font-family:&quot;Arial&quot;,sans-serif;font-size:11pt;line-height:normal;margin:0cm;">Teamplayer Eigenschaften sowie Hands-On Mentalität</li>
</ul>
</div>

Rahmendaten: 
Start: ASAP 
Dauer: 3-6 Monate 
Auslastung: 4-5 Tage / Woche 
Einsatzort: München (Remote nach Rücksprache)
</div>

Interim Buchhaltung (m/w/d)

<div data-wrapper="true" style="font-size:10pt;font-family:Arial;">SAP Application Manager PP/QM (M/F/D)

&nbsp;

Tasks:

<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;&nbsp; &nbsp;Analyzes and defines solutions within the Incident, Change-, Project-Process 
•&nbsp;&nbsp; &nbsp;Understands the business issues, needs, and challenges 
•&nbsp;&nbsp; &nbsp;Suggests areas of improvement 
•&nbsp;&nbsp; &nbsp;Leads projects and initiatives in the PP and QM area 
•&nbsp;&nbsp; &nbsp;Reviews and edits requirements, specifications, business processes, and recommendations related to the proposed solution 
•&nbsp;&nbsp; &nbsp;Develop functional specifications and system design specifications 
•&nbsp;&nbsp; &nbsp;Recommends technical solutions 
•&nbsp;&nbsp; &nbsp;Cooperating with consultants from other modules, such as SD and MM&nbsp; 
•&nbsp;&nbsp; &nbsp;Contributes to driving Biotronik into Digitalization 
•&nbsp;&nbsp; &nbsp;Drive for process harmonization and prepare for a future S4 transformation project</div>

&nbsp;

Qualification:

<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;&nbsp; &nbsp;Very good understanding of SAP PP and QM and related moduleslike MM or SD 
•&nbsp;&nbsp; &nbsp;Bachelor in applied computer science, Information Technology, or similar 
•&nbsp;&nbsp; &nbsp;More than five years of experience in the area of SAP PP/QM&nbsp; 
•&nbsp;&nbsp; &nbsp;Professional experience in projects and rollouts 
•&nbsp;&nbsp; &nbsp;Experience with managing external partner 
•&nbsp;&nbsp; &nbsp;Excellent language skills in English. German is a plus</div>

&nbsp;

Requirements:

Start: asap

Duration: 3-9 months

Capacity: 4-5 days per week

Location: remote</div>

SAP Application Manager PP/QM

<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 NRW&nbsp;sucht aktuell freiberufliche Unterstützung als:

&nbsp;

Senior Manager RA/QA (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;">Regulatory Affairs

	<ul>
		<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Durchführung von Produktregistrierungen&nbsp;</li>
		<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Kommunikation mit zuständigen Behörden und Zertifizierungsstellen&nbsp;</li>
		<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Durchsetzung der Einhaltung notwendiger Vorschriften (IVDR)</li>
		<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Beratungstätigkeiten zur Erlangung und Aufrechterhaltung des Marktzugangs für alle Produkte&nbsp;</li>
		<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Koordinierung und Durchführung der Post Market Surveillance</li>
		<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Beratungstätigkeiten zur Vorbereitung auf die Einhaltung der neuen IVDR</li>
	</ul>
	</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Quality&nbsp;
	<ul>
		<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Weiterentwicklung des Qualitätsmanagementsystems sowie der Qualitätsziele</li>
		<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Durchführung des Management-Review-Prozesses</li>
		<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Tätigkeiten im Rahmen der Qualitätsaufsicht des Produktionsbereiches</li>
		<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Vorbereitung und Koordination von internen und externen Audits</li>
		<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Lieferkettenmanagement </li>
		<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Management von Qualitätssicherungsvereinbarungen</li>
		<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Dokumentation des Änderungsprozesses im Rahmen der Qualitätsmanagementprozesse</li>
		<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">CAPA-Management</li>
	</ul>
	</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">R&amp;D&nbsp;
	<ul>
		<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Koordinierung von Produktentwicklungsprojekten, Designänderungen und Änderungsaufträgen</li>
	</ul>
	</li>
</ul>

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;">Technisches Studium oder vergleichbare Qualifikation</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Min. 5 Jahre Erfahrung im RA/QA Bereich in einem IVD-, Medizinprodukte- oder Pharmaunternehmen</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Erfahrung in Funktionen als QMR und/oder Sicherheitsbeauftragter</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Erfahrung in der In-vitro-Diagnostik &amp; IVRD&nbsp;sowie&nbsp;Bereich der IVD- oder Assay-Entwicklung</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Kenntnisse molekularbiologischer Methoden&nbsp;</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Management-Fähigkeiten: Wünschenswert</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;line-height:normal;margin:0cm;">Erfahrung in RT-PC</li>
</ul>

Rahmendaten:&nbsp;

Start: 16.01.23 spät. 01.03.23

Dauer: 16 Monate

Auslastung: 3 - 5 Tage die Woche

Einsatzort: NRW &amp; remote&nbsp;

&nbsp;
</div>

Senior Manager RA/QA (M/W/D)

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
<div>Process Expert - Planung Biologics Drug Substance Gebäude (m/w/d) 
&nbsp;</div>
&nbsp; 
Aufgaben:

<ul style="unicode-bidi:embed" type="disc">
	<li style="vertical-align:middle; color:#333333">Fachliches Management des Prozess-Teams innerhalb des Projektes</li>
	<li style="vertical-align:middle; color:#333333">Koordination der Projektkommunikation und fachlicher Ansprechpartner für den Prozess in der Zusammenarbeit zwischen dem internen Team und der externen Planungsfirma</li>
	<li style="vertical-align:middle; color:#333333">Fachliche Beratung des Projektleiters und des Projektmanagers im Projektverlauf für den Bereich Prozess</li>
	<li style="vertical-align:middle; color:#333333">Verantwortung über den Prozess (Pilotanlage bis 200 Ltr, Perfusion bis 500 Ltr und Produktion 2000 Ltr) im Rahmen des Projektes. Insbesondere hinsichtlich der Herstellprozesse, ihrer zeit- und räumlichen Abläufe, des Equipments, der Räumlichkeiten, der Inprozesskontrollen, der Analytik, des Personalbedarfs sowie GMP-spezifische Anforderungen</li>
	<li style="vertical-align:middle; color:#333333">Planung der im neuen Gebäude zu integrierende Prozesse (LNP-mRNA, AAV, u.a.), die zugehörige Ausrüstung sowie die spezifischen Anforderungen (z.B. BSL)</li>
</ul>
&nbsp; 
Anforderungen

<ul style="unicode-bidi:embed" type="disc">
	<li style="vertical-align:middle; color:#333333">Abgeschlossenes Studium als Biotechnologe, oder vergleichbar, mit ausgeprägtem Hintergrund bezüglich Prozesstechnologie; Promotion von Vorteil</li>
	<li style="vertical-align:middle; color:#333333">Mehrjährige Projektleitungserfahrung im Bereich der biotechnologischen Produktion (mammalian cell culture, single use bioreactors, perfusion technology, USP, DSP) im pharmazeutischen Umfeld</li>
	<li style="vertical-align:middle; color:#333333">Fundierte GMP Kenntnisse in der biotechnologischen Wirkstoffherstellung (mAB), speziell&nbsp;monoklonaler Antikörper.</li>
	<li style="vertical-align:middle; color:#333333">Kenntnisse der Technischen Gebäudeanforderungen (HVAC, Schleusen, Pufferzubereitung, u.a.) wünschenswert.</li>
	<li style="vertical-align:middle; color:#333333">Sehr gute Deutsch- und Englischkenntnisse in Wort und Schrift – zur Not auch nur Englischkenntnisse</li>
</ul>
&nbsp; 
Rahmendaten

<ul style="unicode-bidi:embed" type="disc">
	<li style="vertical-align:middle; color:#333333">Start: 19.12.2022, spät. 02.01.2023</li>
	<li style="vertical-align:middle; color:#333333">Dauer: 31.03.2023 + mögliche Verlängerung</li>
	<li style="vertical-align:middle; color:#333333">Auslastung: 5 Tage wünschenswert, min.3 Tage erforderlich</li>
	<li style="vertical-align:middle; color:#333333">Location: hauptsächlich remote + Großraum München für notwendige vor Ort Meetings (ca. 1mal pro Woche)</li>
</ul>
</div>

Process Expert - Planung Biologics Drug Substance Gebäude

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Project Manager PMO (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;">
	<div>Operational management of product development projects in the field of diagnostic products from the concept phase to the introduction into serial production</div>
	</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;">
	<div>Leadership of an interdisciplinary team from Development, Quality and Operations (the position is centrally located in the PMO)</div>
	</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;">
	<div>Developing, managing and motivating the project team</div>
	</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;">
	<div>Adherence to time, cost and quality targets in the project as well as transparent communication of changes and risks</div>
	</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;">
	<div>Coordinating all activities to ensure project stakeholder satisfaction</div>
	</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;">
	<div>Reporting to local and international decision making groups</div>
	</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;">
	<div>Maintain project management IT systems in an environment with a high level of project management maturity</div>
	</li>
</ul>

&nbsp;

Qualification:

<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;">
	<div>Completed technical or business management studies</div>
	</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;">
	<div>Assertive motivator with high self-initiative, who forms and leads interdisciplinary teams</div>
	</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;">
	<div>Several years of experience in project management of product development projects, ideally in the Med Tech environment of a multi-national organization</div>
	</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;">
	<div>Expertise in project management methods, incl. certification IPMA Level C upwards or a comparable certification</div>
	</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;">
	<div>Experience with agile methods e.g. Agile Scrum Master or Agile Coach desirable</div>
	</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;">
	<div>Business fluent German and English skills</div>
	</li>
</ul>

&nbsp;

Requirements:&nbsp;

Start: March/April 2023

Duration: 12 months

Capacity: 3-5 days per week

Location: remote

&nbsp;
</div>

PMO 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 Bayern sucht aktuell freiberufliche Beratung als: &nbsp;&nbsp; Experte - Einführung Tax Compliance Management (M/W/D) &nbsp; Aufgaben:
<ul><li style="margin-bottom:4px;list-style-position:inside">Beratung und Begleitung bei der Implementierung eines internen Tax-Compliance-Systems</li><li style="margin-bottom:4px;list-style-position:inside">Projekt- und Beratungsleistung bei der Roll-Out Phase in den jeweiligen Gesellschaften</li><li style="margin-bottom:4px;list-style-position:inside">Beratung bei der Definition sowie Umsetzung von Risiko-Kontroll-Matrizen, Durchführung von Workshops und der Prozess-Dokumentation</li><li style="margin-bottom:4px;list-style-position:inside">Beratung bei der Abbildung und dem Transfer in das interne Risiko-Management-System</li></ul>
<div>Qualifikation:
<ul><li style="margin-bottom:3px;list-style-position:inside">Fundierte, generalistische und praxisrelevante steuerliche Expertise</li><li style="margin-bottom:3px;list-style-position:inside">Projekterfahrung in einer internationalen Matrixorganisation</li><li style="margin-bottom:3px;list-style-position:inside">Erfahrung im Bereich „Steuerliches Risiko-Managements“ (nice to have)</li><li style="margin-bottom:3px;list-style-position:inside">Idealerweise Branchenerfahrung in den Bereichen Banken, Versicherung oder Wirtschaftsprüfung</li><li style="margin-bottom:3px;list-style-position:inside">Deutsch und Englisch verhandlungssichorer</li></ul></div>
Rahmendaten: Start: Ab 02.01.2023 Dauer: ca. 6 Monate Auslastung: 30-40 Std. Einsatzort: Überwiegend Remote (nach Absprache punktuell vor Ort)&nbsp;</div>

Experte - Einführung Tax Compliance Management (m/w/d)

<div data-wrapper="true" style="font-size:10pt;font-family:Arial;">Experte Quality Systems (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;">Durchführung von Tätigkeiten im Zusammenhang mit dem Qualitätsmanagementsystem (QMS)&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;">Implementierung von Folgemaßnahmen im Zusammenhang mit internen 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;">CAPA -Management&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;">Qualitätsüberprüfung von Produktetiketten</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;">Abstimmungstätigkeiten mit Lieferanten und Medline International</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;">Reklamationsbearbeitung&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;">Review von Dokumenten &amp; Systemintegrationsaufgaben&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;">Management von Schulungsanforderungen und Aufzeichnungen/Archiven im Rahmen des QMS</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;">Berufserfahrung im regulierten Umfeld&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;">Nice to have: Ausbildung zum internen Auditor&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;">Gute Kenntnisse von ISO 13485 &amp; ISO 9001 &amp; Medizinprodukteverordnung 2017/745,</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;">Sprachkenntnisse: Deutsch &amp; Englisch&nbsp;</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: Ab sofort

Dauer: 12 Monate

Auslastung: Mind. 4 Tage die Woche

Einsatzort: Baden-Württemberg &amp; remote&nbsp;

&nbsp;</div>

Experte Quality Systems

<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">
Beratungsleistung im Bereich Accounting (M/W/D)

&nbsp;

Aufgaben:

<ul style="unicode-bidi:embed" type="disc">
	<li style="vertical-align:middle">Eigenständige Durchführung von Projekten zur Optimierung der Accounting-Prozesse sowie zur Transformation der EU Finance Shared Services, insbesondere im Hinblick auf Leistungsportfolio, Aufbauorganisation, Prozesse und Systeme. Folgende Projektinhalte sind hierbei relevant:</li>
	<li style="vertical-align:middle">Beratungsleistung bei der qualitäts- und zeitgerechten Erstellung der Monats-, Quartals- und Jahresabschlüsse für ausgewählte Tochtergesellschaften nach IFRS, lokalem Handelsrecht und lokalem Steuerrecht durch das Shared Services Team</li>
	<li style="vertical-align:middle">Beratungsleistung hinsichtlich des Monitorings der SAP-Nebenbücher Bank-, Anlagen-, Debitoren- und Kreditorenbuchhaltung in SAP ECC, Intercompany-Buchungen und Kontenabstimmungen etc. gemäß IFRS, lokaler Rechnungslegung und Steuerrecht im Rahmen des o.g. Projektes</li>
	<li style="vertical-align:middle">Beratungsleistung bei der Sicherstellung der effizienten und zeitgerechten Bearbeitung von Lieferantenrechnungen über den elektronischen Rechnungsworkflow</li>
	<li style="vertical-align:middle">Beratung der EU Finance Shared Services sowie der internen Fachbereiche in der Europa-Zentrale und den lokalen Finance Teams in allen Accounting-bezogenen Fragen</li>
	<li style="vertical-align:middle">Fachlicher Ansprechpartner/-in für Betriebsprüfer, Steuerberater und Wirtschaftsprüfer</li>
</ul>

&nbsp;

Qualifikation:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="box-sizing: border-box;">Wirtschaftswissenschaftliches Studium und/oder vergleichbare kaufmännische Ausbildung</li>
	<li style="box-sizing: border-box;">Langjährige Projekterfahrung im&nbsp;Accounting/ Rechnungswesen eines mittelgroßen oder großen Unternehmens, idealerweise im Pharma-Umfeld und/oder in der Wirtschaftsprüfung</li>
	<li style="box-sizing: border-box;">Berufstitel als Wirtschaftsprüfer und/oder Bilanzbuchhalter/in international von Vorteil</li>
	<li style="box-sizing: border-box;">Langjährige und sehr fundierte Projekterfahrung in der Erstellung von Monats-, Quartals- und Jahresabschlüssen sowie in der Buchung von Intercompany-Geschäftsvorfällen, in der elektronischen Rechnungsverarbeitung und im Asset Accounting</li>
	<li style="box-sizing: border-box;">Langjährige und sehr fundierte Projekterfahrung als Interim Manager mit der Fähigkeit</li>
	<li style="box-sizing: border-box;">Umfangreiche Projekterfahrung in der Projektleitung im Finance-Bereich, idealerweise im Kontext von Transformationen oder der Planung und Implementierung von Shared-Service-Strukturen</li>
	<li style="box-sizing: border-box;">Sehr gute Kenntnisse nach&nbsp;IFRS, HGB und relevantem Steuerrecht erforderlich</li>
	<li style="box-sizing: border-box;">Sehr gute Kenntnisse in&nbsp;SAP R/3 bzw. SAP ERP (MM, FI), sehr gute MS-Office-Kenntnisse erforderlich</li>
	<li style="box-sizing: border-box;">Verhandlungssichere&nbsp;Deutsch- und Englischkenntnisse&nbsp;in Wort und Schrift erforderlich</li>
</ul>

&nbsp;

Rahmendaten:&nbsp;

Start: 05.12.2022, spät. 12.12.2022

Dauer: 30.11.2023

Auslastung: 5 Tage die Woche, min. 2 Tage/Woche vor Ort

Einsatzort: München &amp; remote
</div>

Beratungsleistung im Bereich Accounting

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
<div>Koordinator Übersetzungsprojekte (M/W/D) 
&nbsp; 
Aufgaben:
<ul>
	<li style="list-style-position:inside">Übersetzungen (ENG à DE) primär im Bereich Med. Wiss &amp; Clinical</li>
	<li style="list-style-position:inside">Postediting</li>
	<li style="list-style-position:inside">Review / Qualitätskontrolle von Texten (ENG - DE - ENG) </li>
	<li style="list-style-position:inside">Überprüfen &amp; sicherstellen der korrekten Formatierung</li>
	<li style="list-style-position:inside">Bedarfsanalysen mit dem Fachbereich</li>
	<li style="list-style-position:inside">Abgleich von Dokumenten gemäß dem Brand Plan</li>
</ul>
&nbsp; 
Qualifikation:

<ul>
	<li style="list-style-position:inside">Studium als Übersetzer oder vergleichbar</li>
	<li style="list-style-position:inside">Äußerst detailgenau, organisiert, belastbar</li>
	<li style="list-style-position:inside">Deutsch als Muttersprache, Englisch auf Niveau Muttersprache</li>
	<li style="list-style-position:inside">Sehr gute PC Kenntnisse, sowie mit MS Office 365</li>
	<li style="list-style-position:inside">Sehr gute Kenntnisse mit CAT-Tools (SDL Trados Studio oder ähnlich)</li>
	<li style="list-style-position:inside">Gern gesehen: Erfahrung mit maschineller Übersetzung und Postediting; PM Software aus dem Bereich Übersetzung, FS Pro, Infomapping</li>
	<li style="list-style-position:inside">Freude an Einsatz von neuesten Techniken wie Automation und maschinelle Übersetzung</li>
</ul>
&nbsp; 
Rahmendaten:&nbsp; 
Start: schnellstmöglich 
Dauer: 3 - 6 Monate 
Auslastung: 20&nbsp; - 30 Stunden / Woche 
Einsatzort: remote</div>
</div>

Koordinator Übersetzungsprojekte

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Einer unserer Kunden im Bereich Digital Health in Berlin sucht aktuell freiberufliche Beratung als: 
&nbsp; 
Senior Buchhalter (M/W/D) 
&nbsp; 
Aufgaben:

<ul>
	<li style="font-family: &quot;Open Sans&quot;, sans-serif; font-size: 15px; line-height: normal; margin: 0cm;">Projekt- und Beratungsleistung bei der Erstellung von Monats- und Jahresabschlüssen nach HGB</li>
	<li style="font-family:&quot;Arial&quot;,sans-serif;font-size:11.0pt;line-height:normal;margin:0cm;">Überwachung der operativen Buchhaltungsprozesse und Sicherstellung der durchgeführten Qualität</li>
	<li style="font-family:&quot;Arial&quot;,sans-serif;font-size:11.0pt;line-height:normal;margin:0cm;">Projekt- und Beratungsleistung bei der Gruppenkonsolidierung und Aufbereitung aller relevanten Berichte (Profit &amp; Lost, Balance Sheet, Cash Flow)</li>
	<li style="font-family:&quot;Arial&quot;,sans-serif;font-size:11.0pt;line-height:normal;margin:0cm;">Beratende Unterstützung bei der Prüfung und Genehmigung manueller Journalbuchungen, Rückstellungen und Abgrenzungen in den Haupt- und Nebenbüchern.</li>
	<li style="font-family:&quot;Arial&quot;,sans-serif;font-size:11.0pt;line-height:normal;margin:0cm;">Bereitstellung von angrenzenden Record to Record Finanzfunktionen in hoher Qualität&nbsp;</li>
</ul>

<div>&nbsp;&nbsp;Qualifikation: 
&nbsp;
<ul>
	<li style="font-family:&quot;Arial&quot;,sans-serif;font-size:11.0pt;line-height:normal;margin:0cm;">Fundierte Kenntnisse sowie mehrjährige Berufserfahrung in der Bilanz- / bzw. Finanzbuchhaltung</li>
	<li style="font-family:&quot;Arial&quot;,sans-serif;font-size:11.0pt;line-height:normal;margin:0cm;">Sehr gute Kenntnisse in DATEV sowie dem Konsolidierungsprogramm LUCANET </li>
	<li style="font-family:&quot;Arial&quot;,sans-serif;font-size:11.0pt;line-height:normal;margin:0cm;">Sicher im Abschluss nach HGB / nice to have Kenntnisse in IFRS</li>
	<li style="font-family:&quot;Arial&quot;,sans-serif;font-size:11.0pt;line-height:normal;margin:0cm;">Gute analytische Fähigkeiten und eine Hands-On Mentalität.</li>
	<li style="font-family:&quot;Arial&quot;,sans-serif;font-size:11.0pt;line-height:normal;margin:0cm;">Sehr ergebnisorientiert, strukturiert und organisiert</li>
	<li style="font-family:&quot;Arial&quot;,sans-serif;font-size:11.0pt;line-height:normal;margin:0cm;">Sehr gute Kommunikationsfähigkeiten in Deutsch und Englisch</li>
	<li style="font-family:&quot;Arial&quot;,sans-serif;font-size:11.0pt;line-height:normal;margin:0cm;">Erfahrungen in cross-funktionalen, internationalen Teams sowie in einem dynamischen Umfeld</li>
</ul>
</div>

Rahmendaten: 
Start: ASAP 
Dauer: 4 Monate 
Auslastung: ca. 2-3 Tage / Woche bzw. 10-12 Tage / Monat (ca. 80 - 100 Std.) 
Einsatzort: Remote (Einarbeitungsphase in Berlin)
</div>

Senior Accountant (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: 
 
GMP Expert (M/W/D) 
 
Aufgaben:

<ul>
	<li style="margin-left:8px;list-style-position:inside">Verantwortung für alle relevanten Aufgaben hinsichtlich der bereichsbezogenen GMP-Dokumentation (z. B. SOPs, Prüfanweisungen, Spezifikationen, Durchführungs-, Produktionsprotokolle) </li>
	<li style="margin-left:8px;list-style-position:inside">Pflege der Dokumente aus lokalen und globalen Projekten in Deutsch und Englisch unter Berücksichtigung von Behördenanforderungen für Europa und Amerika. &nbsp;</li>
	<li style="margin-left:8px;list-style-position:inside">Zusammenarbeit mit anderen Standorten und Abgleich der standortspezifischen Dokumente </li>
	<li style="margin-left:8px;list-style-position:inside">Sicherstellung von europäischen, amerikanischen oder anderen Behördenanforderungen &nbsp;</li>
	<li style="margin-left:8px;list-style-position:inside">Nutzung des lokalen und globalen TrackWise-Systems</li>
	<li style="margin-left:8px;list-style-position:inside">Erstellung und Halten von Präsentationen zum eigenen Projektfortschritts in Projektteammeetings</li>
</ul>

<div>Qualifikation:

<ul>
	<li style="margin-left:8px;list-style-position:inside">Mindestens 3-5 Jahre Erfahrung Im GMP-Umfeld </li>
	<li style="margin-left:8px;list-style-position:inside">&nbsp;Projekterfahrung in Change-Management-Prozessen in der pharmazeutischen Industrie </li>
	<li style="margin-left:8px;list-style-position:inside">Solide Kenntnisse über Standortlogistikprozesse wie Wareneingang, Lagerung, Konfektionierung und Verwiegung.</li>
	<li style="margin-left:8px;list-style-position:inside">Fließende Deutsch- und Englisch-Kenntnisse</li>
</ul>
</div>

 
Rahmendaten: 
Start: 01.01.2023 
Dauer: 6 Monate 
Auslastung: 0,6 FTE 
Einsatzort: Remonte 

&nbsp;
</div>

GMP Expert (M/W/D)

<div data-wrapper="true" style="font-size:10pt;font-family:Arial;">Interim Leiter der Fertigung Sondermaschinenbau (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;">Fachliche Führung von 100 Mitarbeitern</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;">Effektivitätssteigerung der aktuellen Fertigung im Bereich Sondermaschinenbau</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;">Begleitung der Einführung eines neuen ERP-Systems</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;">Erfahrung mit GMP-Regularien</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;">Must-have: Erfahrung im Bereich Kleinserienfertigung oder Sondermaschinenbau</li>
</ul>

&nbsp;

Rahmendaten:&nbsp;

Start: ab sofort, spät. Februar 2023

Dauer: 18 Monate

Auslastung: Vollzeit, vor Ort

Einsatzort: Sachsen</div>

Interim Leiter der Fertigung

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

<ul>
	<li style="list-style-position:inside">Interacts with non-financial personnel as well as with internal and external auditors by providing timely and accurate data and communication.</li>
	<li style="list-style-position:inside">Supports all month end closing related finance and logistic processes, including inventory reconciliations</li>
	<li style="list-style-position:inside">Assists in preparation of the financial statements for the annual statutory reporting</li>
	<li style="list-style-position:inside">Manages and develops sales reporting</li>
	<li style="list-style-position:inside">Supports generation of accurate and timely management reports </li>
	<li style="list-style-position:inside">Prepares manual debit notes / credit notes, both to commercial customers as well as Health Care Providers</li>
	<li style="list-style-position:inside">Supports replenishment shipments</li>
	<li style="list-style-position:inside">Supports physical inventory count</li>
	<li style="list-style-position:inside">Prepares new customer set-up and releases credit limit holds</li>
	<li style="list-style-position:inside">Supports CAR-T cell related processes (KITE) from a financial and logistical point of view</li>
</ul>

<div>&nbsp; 
Qualification:

<ul>
	<li style="list-style-position:inside">Two years of experience in finance and/or distributor environment preferred and at least commercial apprenticeship (level of Eidg. Fachausweis) or BA/BS degree in Finance or equivalent.</li>
	<li style="list-style-position:inside">Young Professionals are likewise welcomed</li>
	<li style="list-style-position:inside">Analytical skills</li>
	<li style="list-style-position:inside">Interpersonal skills with the ability to create formal and informal networks within local team as well as the Financial Shared Service Center</li>
	<li style="list-style-position:inside">Able to communicate cross functional both within and outside of the Company while building mutually beneficial relationships.</li>
	<li style="list-style-position:inside">Able to report in concise and solution focused manner key issues to management.</li>
	<li style="list-style-position:inside">Able to work towards due dates, stress resistant and proactive.</li>
	<li style="list-style-position:inside">Strong verbal, written, interpersonal skills with problem resolution orientation.</li>
	<li style="list-style-position:inside">Fluent in German and English (writing and speaking), French would be appreciated.</li>
	<li style="list-style-position:inside">Strong competence with Microsoft Excel (and Word).</li>
</ul>
</div>

&nbsp; 
Requirements:&nbsp; 
Start: asap 
Duration: 12 months 
Capacity: 2 days onsite, 3 days working from home 
Location: Switzerland 
&nbsp; 
&nbsp;
</div>

Junior Finance Specialist

<div data-wrapper="true" style="font-family:Arial; font-size:10pt">Medical Translator (M/F/D)
<div>&nbsp;</div>
<div>Tasks:</div>
<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;">Providing Translations into English language of study related documents </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;">&nbsp;Original Languages can be e.g.: German, French, Dutch, Romanian, Spanish, Czech, Flamish, Polish, Serbian, Croatian </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;">&nbsp;Type of Documents: Clinical Trial Agreements</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;">Usually, contracts are already bilingual or in English</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;">Clinical Trial Application Form and other similar notification forms - in case, only local language submitted </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;">&nbsp;ICF - Only one approved version per country will be translated</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;">CEC - Correspondence, approvals, Membership Lists </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;">&nbsp;LEC- Correspondence, approvals, Membership Lists </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;">&nbsp;CA - &nbsp;Correspondence, approvals </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;">&nbsp;Local Authorities Notification </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;">&nbsp;Local Authorities Approvals </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;">&nbsp;Application letters to and correspondence with EC/CA </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;">&nbsp;Country specific documents required in a specific country for study submission </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;">&nbsp;Essential Correspondence (e.g. CRA to Site; Sponsor to site (German))&nbsp;</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;">Each translated document should be provided together with a statement/certificate of translation, confirming the quality of the translation, with a valid signed and dated by a certified translator and a reviewer.</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;">Volume: approximately 4300 pages</li></ul>
<div>&nbsp;&nbsp;</div>
<div>Requirements:&nbsp;&nbsp;</div>
<div>Start: 01.12.2022</div>
<div>Duration: 6&nbsp;months</div>
<div>Location: &nbsp;Remote</div>
&nbsp;</div>

Medical Translator

<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

<div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Medical Writer (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;"><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; 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">Medical Writing ICFs (Informed Consent Forms, texts for recruiting material for patients and physicians)</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;"><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; 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">Preparation and drafting of patient information/ consent forms, recruitment materials (patients/ physicians) regarding oncology studies:</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;"><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; 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">In the context of oncological studies (clinical trials) based on the legal requirements (GCP, AMG, HWG) and the SOPs an WPs implementing them:</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;"><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; 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">Preparation of patient information / declarations of consent (PatInfos) for newly starting studies as well as recruitment materials for an agreed timeline before the planned submission to the ethics committee: This includes PatInfo for study participants and their relatives, if applicable, etc. as well as potentialy required patient or HCP information material.&nbsp;<span style="-webkit-text-stroke-width:0px; background-color:#ffffff; 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">Estimated review cycles: 2-3 per package</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;"><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; 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">Preparation of amendments to patient information/declarations of consent (PatInfos) for ongoing studies and, if necessary, for other recruitment materials at an agreed timeline before the planned re-submission to the responsible ethics committee: This includes updates for PatInfos for study participants and their relatives, if applicable, as well as potentialy required material (see above).&nbsp;<span style="-webkit-text-stroke-width:0px; background-color:#ffffff; 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">Estimated review cycles: 1-2 per package</li>
</ul>

&nbsp;

Qualification:

<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;"><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; 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">Completed studies in natural sciences</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;"><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; 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">3-5 years experience in clinical science and or in writing of ICFs for interventional studies, e.g. medical writing</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;"><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; 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 regulatory requirements (ICH-GCP, AMG, GCP, EU-CTR) regulations of local / national health authorities</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;"><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; 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 writing of texts for patients in lay-language</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;"><span style="-webkit-text-stroke-width:0px; background-color:#ffffff; 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">German native speaker, fluent in English</li>
</ul>

&nbsp;

Requirements:&nbsp;

Start: 01.12.2022

Duration: until 31.05.2023

Capacity: 12,5 hours per week

Location: remote

&nbsp;
</div>

Medical Writer

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

<ul>
	<li style="margin-left:16px; margin-bottom:11px;list-style-position:inside">Chargenfreigabe</li>
	<li style="margin-left:16px; margin-bottom:11px;list-style-position:inside">Auswertung der Chargenprotokolle</li>
	<li style="margin-left:16px; margin-bottom:11px;list-style-position:inside">Batch Records </li>
	<li style="margin-left:16px; margin-bottom:11px;list-style-position:inside">CAPA-Management</li>
	<li style="margin-left:16px; margin-bottom:11px;list-style-position:inside">Abteilungsübergreifende GMP-Beratung</li>
	<li style="margin-left:16px; margin-bottom:11px;list-style-position:inside">Risikobewertungen für alle Marktprodukte im Verantwortungsbereich</li>
	<li style="margin-left:16px; margin-bottom:11px;list-style-position:inside">Prozessoptimierung in der Produktion</li>
	<li style="margin-left:16px; margin-bottom:11px;list-style-position:inside">Troubleshouting</li>
</ul>

<div>Qualifikation:

<ul>
	<li style="margin-left:16px; margin-bottom:11px;list-style-position:inside">Sachkundige Personen gemäß § 15 AMG</li>
	<li style="margin-left:16px; margin-bottom:11px;list-style-position:inside">Solide Berufserfahrung im Produktionsumfeld</li>
	<li style="margin-left:16px; margin-bottom:11px;list-style-position:inside">Erfahrung im Bereich Orale Arzneimitteln (Brausetabletten, Suspension)</li>
	<li style="margin-left:16px; margin-bottom:11px;list-style-position:inside">Langjährige Erfahrung im Pharma Bereich</li>
</ul>
</div>

Must have: Deutsch, idealerweise auch gute Englischkenntnisse

&nbsp;

&nbsp;

<div style="list-style-position:inside; margin-bottom:11px; margin-left:16px">Rahmendaten: 
Start: asap, spätestens zum 01.01.2023 
Dauer: 6 Monate 
Auslastung1-2 FTE 
Einsatzort: Onsite</div>
</div>

Qualified Person (M/W/D)

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" style="font-family:Arial; font-size:10pt">
Systemingenieur (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;">Realisierung und Justierung von optischen Aufbauten</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;">Messung elektrischer Signale mit Oszilloskop</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;">Verfassen und Review von komplexen Dokumentationen</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;">Lesen von Schaltplänen</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;">Aufnahme und Auswertung von Messdaten</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;">Verfassung und Prüfung von FMEAs, Unterstützung Risikomanagement</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;">Analyse und (Weiter-)Entwicklung der Systemarchitektur</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;">Planung und Durchführung von Verifikationstests- und Messungen</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:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Studium im Bereich Mechatronik, Engineering oder vergleichbar</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;">Profunde, praktische Erfahrung in der Spezifikation und Konzeptentwicklung komplexer Systeme (Hard- und Software)</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;">Erfahrung in der Entwicklung von Geräten in der Medizintechnik</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;">Deutsch und Englisch fließend</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;">Lösungsorientiert, holistischer Blick</li>
</ul>

&nbsp;

Rahmendaten:&nbsp;

Start: ab sofort, spätestens 01.12.2022

Dauer: 6 Monate +

Auslastung: bestenfalls Vollzeit, mindestens 3 Tage / Woche

Einsatzort: Thüringen &amp; Remote&nbsp;
</div>

Systemingenieur

<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 Projektmanager / Change Manager (M/W/D) 
&nbsp; 
Aufgaben:

<ul>
	<li class="paragraph" style="list-style-position:inside;">Koordination, Überwachung und Umsetzung der Projekt- Ressourcen- und Maßnahmenplanung im Lifecycle-Management </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 dem Lifecycle-Team, Moderation der Meetings </li>
	<li class="paragraph" style="list-style-position:inside;">Erstellung und Pflege der Dokumentationen im Änderungsmanagement</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 01.12.22 
Dauer: 6 Monate + 
Auslastung: 4-5 Tage die Woche 
Einsatzort: Thüringen &amp; Remote (nach Einarbeitung flexibel)
</div>

Lifecycle Projektmanager / Change 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 NRW&nbsp;sucht aktuell freiberufliche Unterstützung als: 
&nbsp; 
Experte Category Management&nbsp;(M/W/D) 
&nbsp; 
Aufgaben:

<ul>
	<li>Implementierung / Optimierung eines Category Managements</li>
	<li>Beratung hinsichtlich der Strategieentwicklung einzelner Warengruppen&nbsp;&nbsp;</li>
	<li>Purchase Order Management innerhalb verschiedener Warengruppen&nbsp;</li>
	<li>Optimierung von Einkaufsprozessen&nbsp;</li>
</ul>

Qualifikation:

<ul>
	<li lang="de" style="vertical-align: middle;">Weitreichende Expertise im Bereich Category Management&nbsp;</li>
	<li lang="de" style="vertical-align: middle;">Strategische Expertise sowie Kenntnisse im operativen Beschaffungsmanagement </li>
	<li lang="de" style="vertical-align: middle;">Erfahrung im Bereich des Konzerneinkaufs sowie ein hohes Gesamtprozessverständnis&nbsp;</li>
	<li>Erfahrung im SAP-ERP System</li>
	<li>Sehr gute Englischkenntnisse</li>
</ul>

Rahmendaten: 
Start: Ab sofort / Spätestens 01.01.23 
Dauer: 6 Monate 
Auslastung: 3-5 Tage die Woche 
Einsatzort: Vor Ort &amp; remote&nbsp;

&nbsp;

&nbsp;
</div>

Experte Category Management (m/w/d)

<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 Germany is currently looking for freelance support as:

&nbsp;

Lead Buyer CAPEX (M/F/D) 
&nbsp; 
Tasks:

<ul style="unicode-bidi:embed" type="disc">
	<li style="vertical-align:middle">Lead and drive the sourcing activites for assigned projects with a focus on CAPEX (civil construction &amp; production equipment).</li>
	<li style="vertical-align:middle">Ensure competitive bidding and deliver on-time, on-cost and on-quality Procurement results to projects</li>
	<li style="vertical-align:middle">Manage the relationship with vendors and internal customers, ensuring contracts are established and negotiated as per the project needs</li>
	<li style="vertical-align:middle">Liaise with internal customers and establish a robust &amp; efficient collaborative working interface</li>
	<li style="vertical-align:middle">Maintain close contact to Operational Procurement for best end2end procurement performance</li>
	<li style="vertical-align:middle">Analyze spend data and establish (framework) contracts where beneficial</li>
	<li style="vertical-align:middle">Consult in monitoring performance of key vendors within projects from a risk management perspective</li>
	<li style="vertical-align:middle">Consult to Procurement Strategy definition and subsequent deployment within the region (EU)</li>
	<li style="vertical-align:middle">Consult in collaboration with regions and affiliates to deliver Procurement services</li>
	<li style="vertical-align:middle">Identify and propose process optimization initiatives</li>
	<li style="vertical-align:middle">Respect defined regulatory requirements (e.g. Purchasing Policy, compliance), guidelines and processes</li>
</ul>

&nbsp;

Qualification:

<ul>
	<li style="box-sizing: border-box;">Master or Bachelor degree in engineering (e.g. civil engineer)</li>
	<li style="box-sizing: border-box;">Project experience in indirect procurement plant construction</li>
	<li style="box-sizing: border-box;">Procurement manager with pharma project experience would be nice to have</li>
	<li style="box-sizing: border-box;">Strong negotiation skills combined with contract &amp; legal knowledge</li>
	<li style="box-sizing: border-box;">Project experience in working in cross functional team</li>
	<li style="box-sizing: border-box;">IT Tools: MS Office, SAP MM, eSourcing and affinity to digital tools and IT</li>
	<li style="box-sizing: border-box;">German and English business fluent are necessary</li>
</ul>

&nbsp;

Requirements: 
Start: 07.11.2022 
Duration: until 30.04.2023 
Capacity: 3 days per week 
Location: Greater Area of Munich
</div>

Lead Buyer CAPEX

<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 vor Ort&nbsp; 
Einsatzort: Baden-Württemberg

&nbsp;

&nbsp;

&nbsp;

&nbsp;
</div>

Ingenieur in der Hardwareentwicklung (m/w/d)

<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

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

<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:

2-3x Sales Agent Germany Surgery (D/M/W) 
Regionen: Bayern, Nord-Ost (vielleicht Baden-Württemberg)&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">
<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 cell culture biotech stainless steel is the basic</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: 01.12.22</li>
	<li style="-webkit-font-smoothing: antialiased; box-sizing: border-box; font-style: inherit; font-weight: inherit; margin-left: 25px;">FTE: 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

<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)

<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>

<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

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

<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">
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>