<p><strong>As QC Manager</strong>, you will lead a Quality Control team within a dynamic pharmaceutical CDMO environment. You will be responsible for ensuring high-quality analytical testing standards, regulatory compliance, and efficient laboratory operations while supporting continuous improvement initiatives across the QC function.</p> <p><strong>Start Date</strong>: ASAP</p> <p><strong>Duration</strong>: Permanent Position</p> <p><strong>Place of Work</strong>: Zurich Area</p>
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<p style="line-height:normalmargin-bottom:0cmmargin-right:0cmmargin-top:0cm"><strong>Key Responsibilities</strong></p> <p style="line-height:normalmargin-bottom:0cmmargin-right:0cmmargin-top:0cm">&nbsp</p> <ul> <li> <p style="line-height:normalmargin-bottom:0cmmargin-right:0cmmargin-top:0cm"><span lang="EN-US" xml:lang="EN-US">Lead, coach, and develop a QC team</span></p> </li> <li> <p style="line-height:normalmargin-bottom:0cmmargin-right:0cmmargin-top:0cm"><span lang="EN-US" xml:lang="EN-US">Ensure timely and compliant release testing of raw materials, intermediates, and finished products</span></p> </li> <li> <p style="line-height:normalmargin-bottom:0cmmargin-right:0cmmargin-top:0cm"><span lang="EN-US" xml:lang="EN-US">Oversee analytical testing activities</span></p> </li> <li> <p style="line-height:normalmargin-bottom:0cmmargin-right:0cmmargin-top:0cm"><span lang="EN-US" xml:lang="EN-US">Review and approve analytical data, laboratory documentation, and QC reports</span></p> </li> <li> <p style="line-height:normalmargin-bottom:0cmmargin-right:0cmmargin-top:0cm"><span lang="EN-US" xml:lang="EN-US">Ensure GMP compliance within the QC laboratory environment</span></p> </li> <li> <p style="line-height:normalmargin-bottom:0cmmargin-right:0cmmargin-top:0cm">Manage OOS, deviations, investigations, and CAPAs</p> </li> <li> <p style="line-height:normalmargin-bottom:0cmmargin-right:0cmmargin-top:0cm"><span lang="EN-US" xml:lang="EN-US">Coordinate method transfers, validations, and stability studies</span></p> </li> <li> <p style="line-height:normalmargin-bottom:0cmmargin-right:0cmmargin-top:0cm"><span lang="EN-US" xml:lang="EN-US">Support audits and inspections from customers and authorities</span></p> </li> <li> <p style="line-height:normalmargin-bottom:0cmmargin-right:0cmmargin-top:0cm"><span lang="EN-US" xml:lang="EN-US">Collaborate closely with QA, Production, and external partners</span></p> </li> <li> <p style="line-height:normalmargin-bottom:0cmmargin-right:0cmmargin-top:0cm"><span lang="EN-US" xml:lang="EN-US">Drive continuous improvement initiatives within laboratory operations</span></p> </li> <li> <p style="line-height:normalmargin-bottom:0cmmargin-right:0cmmargin-top:0cm"><span lang="EN-US" xml:lang="EN-US">Ensure proper maintenance, calibration, and qualification of laboratory equipment</span></p> <p style="line-height:normalmargin-bottom:0cm">&nbsp</p> </li> </ul>
<p style="line-height:normalmargin-bottom:0cmmargin-right:0cmmargin-top:0cm"><strong>Candidate Profile</strong></p> <p style="line-height:normalmargin-bottom:0cmmargin-right:0cmmargin-top:0cm">&nbsp</p> <ul> <li> <p style="line-height:normalmargin-bottom:0cmmargin-right:0cmmargin-top:0cm"><span lang="EN-US" xml:lang="EN-US">Degree in Chemistry, Pharmaceutical Sciences, or related field</span></p> </li> <li> <p style="line-height:normalmargin-bottom:0cmmargin-right:0cmmargin-top:0cm"><span lang="EN-US" xml:lang="EN-US">Several years of experience in Quality Control within the pharmaceutical, biotech, or CDMO industry</span></p> </li> <li> <p style="line-height:normalmargin-bottom:0cmmargin-right:0cmmargin-top:0cm"><span lang="EN-US" xml:lang="EN-US">Previous leadership or team management experience</span></p> </li> <li> <p style="line-height:normalmargin-bottom:0cmmargin-right:0cmmargin-top:0cm"><span lang="EN-US" xml:lang="EN-US">Strong GMP knowledge and understanding of regulatory requirements</span></p> </li> <li> <p style="line-height:normalmargin-bottom:0cmmargin-right:0cmmargin-top:0cm"><span lang="EN-US" xml:lang="EN-US">Hands-on experience with analytical laboratory methods and equipment</span></p> </li> <li> <p style="line-height:normalmargin-bottom:0cmmargin-right:0cmmargin-top:0cm"><span lang="EN-US" xml:lang="EN-US">Experience with investigations, deviations, and CAPA processes</span></p> </li> <li> <p style="line-height:normalmargin-bottom:0cmmargin-right:0cmmargin-top:0cm"><span lang="EN-US" xml:lang="EN-US">Structured, solution-oriented, and proactive working style</span></p> </li> <li> <p style="line-height:normalmargin-bottom:0cmmargin-right:0cmmargin-top:0cm"><span lang="EN-US" xml:lang="EN-US">Strong communication and stakeholder management skills</span></p> </li> <li> <p style="line-height:normalmargin-bottom:0cmmargin-right:0cmmargin-top:0cm"><span lang="EN-US" xml:lang="EN-US">Fluent in English and German (written and spoken)</span></p> </li> </ul> <p style="line-height:normalmargin-bottom:0cmmargin-right:0cmmargin-top:0cm">&nbsp</p> <p style="line-height:normalmargin:0cm 0cm 0cm 40px"><span lang="EN-US" xml:lang="EN-US">Job ID 19014</span></p>

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