Senior QA Specialist - Project Manager LZAJP00004170
Start date: Immediately:
End date: 31.12.2024
Location: Valais, on site
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 present during their GMP audits
Requirements
- A degree in Life Science (microbiology, biotechnology, chemistry)
- Relevant experience in the biopharmaceutical industry, ideally in GMP area
- Strong communication skills, experience in working with stakeholders from different departments
- Experience with TrackWise, SAP, LIMS and DMS is a plus
- Fluency in English
About the company
