Senior QA Specialist – Project Manager (f/m/d) (Ref.Nr. LA3179)
Brine
- Valais
- CDI
- Temps-plein
- responsible to ensure production of API`s is in accordance with Good Manufacturing Practice (GMP) (Bioconjugates),
- 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.
- be the quality contact for the companies clients and will present during their GMP audits.
- a degree in Life Science (microbiology, biotechnology, chemistry)
- minimum 3-5 years 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 (writing and speaking) is required for stakeholder communication, German skills on B1 level are required to interact with colleagues daily.