Duration : 15 / 09 / 2024 to 31 / 03 / 2025
Key responsibilities :
* Review executed electronic and/or manufacturing protocol for compliance to GMP. Support implementation/revision of manufacturing protocols for GMP manufacturing.
* Ensure that internal/external GMP standards and regulatory requirements are adhered to in projects.
* Participate in cross-functional investigations to determine impact to product quality and the definition of associated corrective measures.
* Represent the Quality Unit in cross-functional teams. Make independent quality-related decisions based on regulatory and compliance knowledge and provide independent quality support to project teams.
* Review and approve validation documents.
Key requirements :
* Degree in Biology, Chemistry, Biotechnology, Life Science or other related field or experience in the field of pharmaceutical industry.
* Previous experience in GMP regulated pharmaceutical industry is an advantage.
* English fluency and good command of German is an advantage.
* Ability to prioritize and manage work to critical project timelines in a fast-paced environment.
* Excellent verbal, written and interpersonal communication skills.
Please note that since the position is in Switzerland, we are only able to work with people who have a European passport or already have a Swiss working permit/citizenship.
Sthree Switzerland is acting as an Employment Business in relation to this vacancy.
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