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

Apply to join our team.

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

Are you interested in this project?

<div data-wrapper="true" dir="ltr" style="font-size:10pt;font-family:Arial;">Dokumentenspezialist (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;">Umgang mit Qualifizierungsdokumenten 

	<ul style="list-style-type:circle">
		<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;">Prüfung auf Vollständigkeit</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;">Genehmigung</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;">Archivierung </li>
	</ul>
	</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;">Führen und Abarbeitung von Qualifizierungslisten</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;">Erstellung bzw. Optimierung von SOPs &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;">Trainingsunterlagen
	<ul style="list-style-type:circle">
		<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;">Tracking von Trainingslisten</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;">Sicherstellen, dass alle Mitarbeiter trainiert sind</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;">Archivierung von Trainingsunterlagen</li>
	</ul>
	</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;">Auditobservations
	<ul style="list-style-type:circle">
		<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;">Tracking von Listen zur Optimierung des Qualitäts-Management-Systems</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;">Initiierung von ergänzenden Aktivitäten zur Behebung von Abweichungen</li>
	</ul>
	</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;">Batchrecord (perspektivisch NACH der Qualifizierungsphase)
	<ul style="list-style-type:circle">
		<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Review</li>
	</ul>
	</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 in QA/QC sowie GMP</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;">Verständnis von QC bzw. Produktionsprozessen in der Pharmaindustrie</li>
</ul>

&nbsp;

Rahmendaten:&nbsp;

Start: Mitte Januar /Anfang Februar 2024

Dauer: 3-4 Monate

Auslastung: ca. 4-5 Tage die Woche

Einsatzort: Frankfurt am Main</div>

Dokumentenspezialist (m/w/d)

<div data-wrapper="true" dir="ltr" style="font-size:10pt;font-family:Arial;">VDE-zertifizierter Meister-Elektroniker (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;">Analyse / Prüfung der VDE-Konformität der Anlagen und Installationen eines Labors</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Verfassen eines Analyseberichtes</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Falls die Analyse Abweichungen ergibt: Verfassen eines neuen VDE-konformen Designs</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Anschließend ggf. Leitung der Durchführung von Anpassungen an das neue Design</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;">Meister in Elektrotechnik</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;">VDE-Zertifiierung</li>
</ul>

&nbsp;

Rahmendaten:&nbsp;

Start: so bald wie möglich

Dauer &amp; Auslastung: Circa 8 Arbeitstage für die Vorbereitung, Durchführung und Verfassen der Analysen. Falls notwendig circa 20 Arbeitstage für das Verfassen des neuen Designs

Einsatzort: Baden-Württemberg &amp; remote</div>

Analyse Projekt VDE-zertifizierter Elektroniker

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

&nbsp;

Tasks:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Designs, develops, and implements marketing program strategies to support the organization's products. </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;">Uses specific marketing strategies and media (e.g., print, broadcast, digital) to launch and position products. </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;">Identifies and implements marketing strategies and programs in collaboration with sales and technical teams.</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;">Track record in developing and implementing multi-channel marketing strategies</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Extensive Experience in Salesforce Marketing Cloud Journey builder and/or Automation Studio/Data Cloud - mandatory</li>
</ul>

&nbsp;

Requirements:&nbsp;

Start: asap

Duration: 9 months +

Capacity: 5 days per week

Location: US, fully remote

&nbsp;</div>

Marketing Specialist

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" dir="ltr" style="font-family:Arial; font-size:10pt">
HSE Manager Gefahrenstoffe &amp; Chemikalien (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;">Entwicklung von Strategien und lokale Umsetzung von Prozessen im Bereich HSE, besonders Gefahrenstoffe &amp; Chemikalien</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;">Verantwortlich für Prozesssicherheit inklusive Reporting</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;">Eruieren zulassungsrelevanter Inhalte inkl. nötiger Tests</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;">Maintenance von REACH Dossiers</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;">Mitarbeiterschulungen (Prozesse &amp; Kultur)</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;">Relevanter Ausbildungshintergrund Engineering</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;">Aktuelle und sofort abrufbare Kenntnisse für HSE Richtlinien/Gesetzgebung EU und Deutschland</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;">Explizit sehr gute Kenntnisse im Bereich REACH, GHS/CLP)</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;">Sehr gute Fähigkeiten in den Bereich Kommunikation</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;">Projektmanagement &amp; Überzeugungskraft</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;">Idealerweise zertifizierte Fachkraft für Arbeitssicherheit</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;">Gutes Englisch (Wort &amp; Schrift)</li>
</ul>

&nbsp;

Rahmendaten:&nbsp;

Start: ab sofort, spät. 02/24

Dauer: 3-4 Monate

Auslastung: mind. 30 Stunden / Woche (idealerweise Vollzeit)

Einsatzort: vor Ort NRW &amp; remote
</div>

HSE Manager Gefahrenstoffe & Chemikalien

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

&nbsp;

Tasks:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="margin-bottom:11px;list-style-position:inside">Execute solid sustainability strategy, ensuring alignment with the core principles and vision of the company</li>
	<li style="margin-bottom:11px;list-style-position:inside">Lead and manage the cross-functional, interdisciplinary teams</li>
	<li style="margin-bottom:11px;list-style-position:inside">Continuous monitoring and reporting of program/projects status and progress</li>
	<li style="margin-bottom:11px;list-style-position:inside">Lead pioneering research and innovation to develop and execute sustainable technologies and solutions</li>
	<li style="margin-bottom:11px;list-style-position:inside">Identify new topics for cooperation</li>
	<li style="margin-bottom:11px;list-style-position:inside">Define and track sustainability KPIs, reporting to stakeholder both within and outside the company</li>
	<li style="margin-bottom:11px;list-style-position:inside">Guarantee adherence to relevant environmental laws and sector-specific sustainability standards.</li>
	<li style="margin-bottom:11px;list-style-position:inside">Providing relevant contributions to internal and external communication to strengthen sustainability in the corporate culture and make the company’s activities visible</li>
	<li style="margin-bottom:11px;list-style-position:inside">Keep abreast of the latest environmental trends, practices, and technological advancements to continually refine the sustainability strategies of the company.</li>
</ul>

&nbsp;

Qualification: 
&nbsp;

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="margin-bottom:11px;list-style-position:inside">University Degree in sustainability or environmental discipline.</li>
	<li style="margin-bottom:11px;list-style-position:inside">Solid Background in the sustainability management (at least 3 years)</li>
	<li style="margin-bottom:11px;list-style-position:inside">Deep understanding of GRI, TCFD, CSRD, CDP, SBTi or SDGs and practical experience in their corporate application</li>
	<li style="margin-bottom:11px;list-style-position:inside">Comprehensive knowledge of environmental laws, norms, and best practices.</li>
	<li style="margin-bottom:11px;list-style-position:inside">Strong expertise in management of programs/projects, allocating needed project resources, managing timelines and budget</li>
	<li style="margin-bottom:11px;list-style-position:inside">Solid leadership and organizational skills</li>
	<li style="margin-bottom:11px;list-style-position:inside">Excellent communication skills on all management levels</li>
</ul>

&nbsp;

Requirements:&nbsp;

Start: ASAP

Duration: 6 months

Capacity: 3-5 days per week

Location: Hessen

&nbsp;</div>

Project Manager Sustainability

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

&nbsp;

Tasks:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Contribute to the develop of risk assessments by review and comprehension of operating procedures, regulatory guidance, in-house data and scientific literature under general direction.</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;">Assist in the conduct of globally distributed projects as needed.</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Develop solutions for problems and challenges in a project under supervision.</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;">Assist with authorship and review of scientific reports and risk assessments.</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;">Master degree, or equivalent in Science related field.</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;">An advanced degree (PhD) in Science, or equivalent is preferred. </li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Experience in virology, cell and gene therapy, bioanalytics, cell biology, biotechnology, or similar field is highly preferred.</li>
</ul>

&nbsp;

Requirements:&nbsp;

Start: 12/01/23

Duration: 12 months

Capacity: 5 days per week

Location: Illinois, US and Remote

&nbsp;</div>

Principal Scientist

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

<ul>
	<li style="margin-bottom:11px;list-style-position:inside">Schnittstelle intern wie extern für medizinische Fragestellungen zu Unternehmensprodukten </li>
	<li style="margin-bottom:11px;list-style-position:inside">Beratung der kommerziellen Abteilungen zu allen anfallenden klinischen Fragestellungen</li>
	<li style="margin-bottom:11px;list-style-position:inside">Mitarbeit bei der Durchführung von klinischen Studien und Bewertung des Produktportfolio</li>
	<li style="margin-bottom:11px;list-style-position:inside">Pflege und Mitgestaltung des globales wissenschaftliches </li>
	<li style="margin-bottom:11px;list-style-position:inside">Schulung und Coaching der Kollegen zu medizinischen Kenntnissen </li>
	<li style="margin-bottom:11px;list-style-position:inside">Steuerung des externen Medical Advisory Board </li>
	<li style="margin-bottom:11px;list-style-position:inside">&nbsp;Konzeption eines wissenschaftlichen Programms von Symposien und</li>
	<li style="margin-bottom:11px;list-style-position:inside">Planung und Moderation von Konferenzen mit Meinungsbildnern </li>
</ul>

<div>&nbsp; 
Qualifikation:

<ul>
	<li style="margin-left:16px; margin-bottom:11px;list-style-position:inside">Medizinischer Background (Humanmedizin oder Naturwissenschaften mit Promotion)</li>
	<li style="margin-left:16px; margin-bottom:11px;list-style-position:inside">Track Record als Medical Affairs Director oder in einer ähnlichen Position in der Medizintechnik </li>
	<li style="margin-left:16px; margin-bottom:11px;list-style-position:inside">Idealerweise Expertise in der Ernährungsmedizin </li>
	<li style="margin-left:16px; margin-bottom:11px;list-style-position:inside">Flughöhe/Standing für tiefgreifende Gespräche mit Fachexperten </li>
	<li style="margin-left:16px; margin-bottom:11px;list-style-position:inside">Fließend in Deutsch und Englisch/ Internationale Erfahrung vorhanden </li>
</ul>
</div>

&nbsp; 
Rahmendaten:&nbsp; 
Start: asap, spätestens zum 01.01.24 
Dauer: 6 Monate 
Auslastung: 1 FTE, 4-5 Tage 
Einsatzort: Onsite/Remote 

&nbsp;

&nbsp;
</div>

Medical Affairs Director MedTech (m/w/d)

<div data-wrapper="true" dir="ltr" style="font-size:10pt;font-family:Arial;">QA Associate (M/F/D)
&nbsp;
Tasks:
<ul style="margin-bottom:0cm; margin-top:0cm" type="disc"><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Ensures that qualification, validation, and technical protocols, and reports comply with site SOPs. </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;">Provides review and approval of 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;">Provides QA oversight to equipment qualification, computer system validation (e-compliance), method, process, and cleaning validation including revalidation and re-evaluation.</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;">Provides validation documentation lifecycle oversight.</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;">Utilizes data analysis skills and statistical tools to interpret results in support of acceptance criteria and regulatory requirements.</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;">Interfaces with customers and partners on quality-related issues, participates as the QA representative on multi-functional continuous improvement teams and ensures efficient and timely project support.</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;">Acquires and maintains knowledge of current local and international regulatory and legislative requirements and trends to ensure that expert advice and appropriate technical support on all quality/compliance-related matters are provided to the site.</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;">In addition, ensures Good Engineering Practices are followed according to GAMP, ISPE, and company standards.</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;">The QA-Engineering contractor will have QA oversight on validation deliverables in QC, Bulk Manufacturing, and Fill Finish collaborating with CQV (Commissioning Qualification and Validation), MS&amp;T (Manufacturing Science and Technology), AS&amp;T (Analytical Science and Technology), QC (Quality Control), Manufacturing, and Engineering.</li></ul>
&nbsp;
Qualification:
<ul style="margin-bottom:0cm; margin-top:0cm" type="disc"><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Bachelor’s degree in Science or Engineering discipline preferred or equivalent experience in biotech or pharmaceutical industry.</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">5+ years’ experience in Quality Assurance and/or in a GMP regulated environment within the pharmaceutical industry or equivalent.</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;">Incumbent should possess a solid understanding of computer system validation and equipment qualification.</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;">Experience in method, cleaning and process validation and associated deliverables including international regulatory and legislative requirements is preferred.</li><li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Acquires and maintains knowledge of current local and international regulatory and legislative requirements and trends to ensure that expert advice and appropriate technical support on all quality/compliance related matters are provided to the site.</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;">In addition, ensures Good Engineering Practices are followed according to GAMP, ISPE, and company standards.</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;">Team player developing relationships with key individuals in the work teams, offering assistance and sharing resources with other team members.</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;">Experience with e-Compliance/computer validation preferably in a GMP regulated environment within the pharmaceutical industry.</li></ul>
&nbsp;
Requirements:&nbsp;
Start: 12/04/23
Duration: 4 months
Capacity: 5 days per week
Location: Onsite in NC &amp; Remote</div>

Quality Assurance Associate (QA-Engineering)

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

<ul>
	<li style="margin-bottom:11px;list-style-position:inside">&nbsp;Durchführung von Sales-Kampagnen und Aktivitäten zur Gewinnung von Neukunden im Gesundheitssektor </li>
	<li style="margin-bottom:11px;list-style-position:inside">Verkauf von Content (Print, Newsletter, Podcasts, Informationsdienste, CMR-Webinare) als Produkt </li>
	<li style="margin-bottom:11px;list-style-position:inside">Aufbau eines Netzwerks und Nutzung eines vorhandenen Netzwerks im Pharmabereich zur Erweiterung des Kundenkreises </li>
	<li style="margin-bottom:11px;list-style-position:inside">Akquisition und anschließend Betreuung von Neukunden und Kooperationspartnern</li>
	<li style="margin-bottom:11px;list-style-position:inside">Optimierung des Konzepts zur Kundengewinnung </li>
	<li style="margin-bottom:11px;list-style-position:inside">Business Development, Besuch von Messen und Kongressen</li>
</ul>

<div> 
&nbsp; 
Qualifikation:

<ul>
	<li style="margin-bottom:11px;list-style-position:inside">&nbsp;Sales Profi mit nachweisbarem Erfolg im Business Development &nbsp;</li>
	<li style="margin-bottom:11px;list-style-position:inside">Vorhandenes Netzwerk in der Pharmabranche, und im Bereich Life Sciences </li>
	<li style="margin-bottom:11px;list-style-position:inside">Entrepreneur Mindset, Erfolgsorientiert </li>
	<li style="margin-bottom:11px;list-style-position:inside">Track Rekord im Business Development&nbsp;</li>
</ul>
</div>

 
Rahmendaten:&nbsp; 
Start: 01.12.2023, spätestens am 01.01.2024 
Dauer: 6 Monate 
Auslastung: 2 Tage/ Woche 
Einsatzort: Remote &amp; vor Ort
</div>

Projekt Manager Business Development (M/W/D)

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" dir="ltr" style="font-family:Arial; font-size:10pt">
Qualified Person (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;">Überwachung des Freigabeprozesses und Sicherstellung aktueller, korrekter und GMP-konformer Standards und Verfahren.</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;">Genehmigung von Herstellungsprotokollen und korrekte Handhabung von Freigabemustern.</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;">Funktion als Qualified Person gemäß EU-GMP-Leitfaden, inklusive Zertifizierung für Chargenfreigabe und lokaler Vorschriften.</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Freigabe von importiertem Wirkstoffen gemäß EU-GMP-Leitfaden.</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;">Qualitätsüberwachung durch Dokumentenprüfung und Audits.</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Sicherstellung der Einhaltung von Herstellungserlaubnis-Anforderungen</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;">Anwendung hoher ethischer Standards im Kunden- und Behördenkontakt.</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;">Zusammenarbeit mit verschiedenen Abteilungen für effektives Qualitätsmanagement und GMP-Konformität.</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;">Bereitstellung regulatorischer Unterstützung für Anträge, Verlängerungen, Variationen.</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;">Treffen von Entscheidungen bei Produkt-Rückrufen.</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;">Teilnahme am Qualitätsmanagementsystem durch Dokumentenerstellung und -prüfung, um lokale und EU-GMP Anforderungen zu erfüllen.</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;">Durchführung von QP-bezogenen Audits bei externen Lieferanten nach Bedarf.</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;">Erforderliche Qualifikation zur Anerkennung als Qualified Person gemäß §15 AMG.</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;">Theoretisches und praktisches Wissen in Biopharmazie, Herstellung, Qualitätskontrolle und Freigabe.</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Tiefes Verständnis von Arzneimittelrecht, Qualitätsmanagement und QP-Pflichten.</li>
	<li style="margin-top:0cm;margin-right:0cm;margin-bottom:0cm;margin-left:0cm;line-height:normal;font-size:15px;font-family:&quot;Open Sans&quot;,sans-serif;">Kenntnisse in Medizinischer Chemie oder biopharmazeutischem Fachwissen.</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;">Umfassendes Verständnis der Herstellung und Lieferkette.</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;">Führungs- und Kommunikationsfähigkeiten.</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;">Deutsch und Englisch fließend.</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;">Fähigkeit, unter Druck souveräne Entscheidungen zu treffen und bei Fehlern entschlossen zu handeln.</li>
</ul>

&nbsp;

Rahmendaten:&nbsp;

Start: ASAP

Dauer: ca. 6 Monate

Auslastung: 3 Tage die Woche

Einsatzort: NRW
</div>

Qualified Person (m/w/d)

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" dir="ltr" style="font-family:Arial; font-size:10pt">
Batch Record Experte (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;">Durchführung von Batch Record Reviews</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Verantwortlich für die Überprüfung von Chargenprotokollen von Nahrungsergänzungmittel, Kosmetika und Humanmedizinischen Produkten</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Koordinierung mit Kollegen aus dem Bereich Qualität und funktionsübergreifenden Abteilungen (z. B. externe Fertigung, Logistik und Planung) in Bezug auf den Chargenstatus, den Status des Analysezertifikats</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Vorbereitung zur Chargenfreigabe&nbsp;</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Bearbeiten und Erstellen von Batchtabellen</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Prozessoptimierung in enger Zusammenarbeit mit FvPs&nbsp;</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;">Fundierte analytische Kenntnisse und Fähigkeit Abweichungen von Qualitätsstandards festzustellen&nbsp;</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">strukturierte und präzise Arbeitsweise&nbsp;</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Erfahrung mit Stabilitätsstudien und dem Batch Release Prozess (Pharma, Nahrungsergänzung, Kosmetika)&nbsp;</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Kenntnisse hinsichtlich regulatorischer Aspekte (z.B. Protokollerstellung)&nbsp;</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">Fliessende Deutschkenntnisse&nbsp;</li>
	<li style="margin: 0cm; line-height: normal; font-family: &quot;Open Sans&quot;, sans-serif;">entsprechender akademischer Hintergrund (Pharmazie, Chemie) sollte gegeben sein&nbsp;</li>
</ul>

&nbsp;

Rahmendaten:&nbsp;

Start: ab sofort&nbsp;

Dauer: 6 Monate (Möglichkeit auf Verlängerung oder Festanstellung)&nbsp;

Auslastung: 3 -5 Tage/ Woche&nbsp;

Einsatzort: Grossraum St. Gallen&nbsp;

&nbsp;
</div>

Batch Record Expert

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" dir="ltr" style="font-family:Arial; font-size:10pt">Projektingenieur Prozessequipment(m/w/d)
&nbsp;
Hintergrund:&nbsp;Der Kunde führt eine Machbarkeits- und Konzeptstudie für die Errichtung eines neuen Produktionsgebäudes zur Herstellung von hochpotenten Antikörper-Wirkstoff-Konjugaten durch.
&nbsp;
Aufgaben:
<ul style="margin-bottom:0cm; margin-top:0cm" type="disc"><li style="box-sizing: border-box;">Projektierung von Prozessequipment im Rahmen eines Investment-Projektes zur Errichtung von Produktionskapazitäten im Bereich der Biokonjugation (Herstellung von Antikörper-Wirkstoff-Konjugaten aus monoklonalen Antikörpern und chemisch-synthetischen Wirkstoffen) und Fill&amp;Finish</li><li style="box-sizing: border-box;">Erarbeiten von Konzepten und Spezifikationen (URS) für Neuanlagen</li><li style="box-sizing: border-box;">Zusammenarbeit mit einer externen Planungsfirma, zunächst in den Projektphasen Machbarkeits- und Konzeptstudie (LPh 1-2 HOAI) mit Fokus auf Fragestellungen zum Prozessequipment und Layout</li><li style="box-sizing: border-box;">Zusammenarbeit bei der technischen Planung / Auslegung des Prozessequipments wie bspw. Isolatoren, Fülllinien, Gefriertrockner, Autoklaven, Ultra-/Diafiltration, Puffertanks, Rührtanks etc.</li><li style="box-sizing: border-box;">Schnittstellenklärung zwischen den Gewerken Elektro, TGA, Prozess, Bau, Reinstmedien und Logistik</li><li style="box-sizing: border-box;">Sicherstellung der GMP-Compliance und Einhaltung von EHS-Vorgaben (OEB5/6 Stoffe werden verarbeitet)</li><li style="box-sizing: border-box;">Review/ teilweise Erstellung relevanter Dokumentation und Präsentationen</li><li style="box-sizing: border-box;">Option zur Fortführung der Tätigkeit in den weiteren Leistungsphasen Basic Design, Detail Design und Inbetriebnahme / Qualifizierung</li></ul>
&nbsp;
Qualifikation:
<ul style="margin-bottom:0cm; margin-top:0cm" type="disc"><li style="box-sizing: border-box;">Abgeschlossenes Studium der Ingenieurswissenschaften oder vergleichbare Qualifikation von Vorteil</li><li style="box-sizing: border-box;">Mehrjährige (&gt;3 Jahre) Berufserfahrung in der Planung &amp; Realisierung von Projekten im Biotechnologiebereich (USP, DSP, mAb und/oder Biokonjugation) oder Fill&amp;Finish und aseptischer Fertigung</li><li style="box-sizing: border-box;">Fundierte Projektmanagementkenntnisse</li><li style="box-sizing: border-box;">Erfahrung in der Zusammenarbeit mit Generalplanern wünschenswert</li><li style="box-sizing: border-box;">GMP-Kenntnisse und Erfahrung im regulatorischen Umfeld der Pharma- oder Biotechnologie</li><li style="box-sizing: border-box;">Eigenständige, strukturierte und zielorientierte Arbeitsweise, Organisationsvermögen, Teamfähigkeit, Flexibilität</li><li style="box-sizing: border-box;">Affinität zu digitalen und innovativen Technologien</li><li style="box-sizing: border-box;">Gute Kenntnisse der gängigen MS Office Anwendungen</li><li style="box-sizing: border-box;">Sehr gute Deutsch- und Englischkenntnisse in Wort und Schrift</li></ul>
&nbsp;
Rahmendaten:&nbsp;
Start: 01.10.2023
Dauer: bis 30.04.2024
Auslastung:4-5 Tage / Woche
Einsatzort: Pfaffenhofen &amp; remote
&nbsp;</div>

Projektingenieur Prozessequipment

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

&nbsp;

Tasks:

<ul style="margin-bottom:0cm; margin-top:0cm" type="disc">
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Develop and execute comprehensive project plans for clinical trials across all phases.</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;">Lead cross-functional project teams, ensuring effective communication and collaboration.</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;">Serve as the primary point of contact for clients, maintaining regular communication and addressing project updates and timelines.</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;">Ensure compliance with regulatory guidelines, Good Clinical Practice (GCP), and standard operating procedures (SOPs).</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;">Identify and manage potential risks, implementing proactive risk management measures.</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;">Oversee project budgets and resource allocation, tracking expenses and reporting budget status to stakeholders.</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;">Minimum of 5 years of clinical project management experience in a CRO or pharmaceutical/biotech organization.</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Strong understanding of clinical trial processes, regulations, and ICH-GCP guidelines.</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Excellent leadership, communication, and negotiation skills.</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;">Proven ability to manage multiple clinical trials simultaneously and deliver projects within established timelines and budgets.</li>
	<li style="font-family:&quot;Open Sans&quot;,sans-serif;font-size:16px;line-height:normal;margin-bottom:0cm;margin-left:0cm;margin-right:0cm;margin-top:0cm;">Proficiency in project management tools and 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;">Nice to have: Project Management Certificate</li>
</ul>

&nbsp;

Requirements:&nbsp;

Start: asap, latest 1st of September

Duration: 6 months

Capacity: 2.5-5 days per week

Location: Remote, but has to work in different time zones (East- and Westcoast, Europe)</div>

Clinical Project Manager

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

&nbsp;

Tasks:

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

&nbsp;

Qualification:

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

&nbsp;

Requirements:&nbsp;

Start: 01/06/23

Duration: 6 months +

Capacity: 3-5 days per week

Location: Onsite in Missouri &amp; Remote

&nbsp;
</div>

Project Lead MDR

<title>Description Posting &amp; Mailing rich text editor</title><div data-wrapper="true" 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 
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