QA Specialist / Batch Record Review
Location: Valais
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 German good command is an advantage
* Ability to prioritize and manage work to critical project timelines in a fast-paced environment.
* Excellent verbal, written and interpersonal communications skills
If this role is of interest to you, or anyone from your network, feel free to send me your CV and expected hourly rate for immediate consideration. I am specialised recruiter taking care of various projects within the Life Sciences Industry.
*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.