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vor 4 Wochen
Direct message the job poster from Consultys Suisse.
For more than 19 years, through our consulting and engineering activities, we have supported our clients throughout the entire lifecycle of biotechnology, pharmaceutical and device products.
Part of an organization of more than 750 employees, Consultys Switzerland supports and develops talented individuals recognized for their technical and scientific expertise. Our activities allow us to be present in both French-speaking and German-speaking Switzerland, with agencies in Lausanne and Basel.
At Consultys, we're proving that it's possible to combine people and performance.
Much more than concepts, our 3 values "Respect, Recognition and Transparency" guide us and are the foundation of our history, the heart of our group's success.
As part of our development, we are recruiting a Senior QA Specialist to join our teams in the French-Speaking part of Switzerland.
Responsibilities:- Be responsible to ensure production of API's is in accordance with Good Manufacturing Practice (GMP).
- Support the contract manufacturing and advise members of development, production and analytical departments on all aspects of GMP.
- Responsible for checking manufacturing documentation for conformity, processing of change controls and reviewing and approving of deviations and OOS-results.
- In addition, you will be the quality contact for our clients, and will be present during their GMP audits.
- Degree in Life Science (microbiology, biotechnology, chemistry).
- Relevant experience in the biopharmaceutical industry, ideally in GMP area.
- 5 years experience in Quality Assurance.
- Strong communication skills, experience in working with stakeholders from different departments.
- Experience with TrackWise, SAP, LIMS and DMS is a plus.
- Fluency in English (writing and speaking).
Associate
Employment Type:Full-time
Job Function:Quality Assurance
Industries:Business Consulting and Services and Biotechnology Research
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