Senior QA Specialist – Project Manager
On behalf of our client, a leading international biotechnology company based in Visp, Swisslinx is looking for a Senior QA Specialist in the quality assurance (Bioconjugates) team.
Contract type: Contract
Start Date: ASAP
Location: Visp
Workload: 100%
Work type: Hybrid
Duration: end of 2024 (possibility of extension)
Your mission
â?¢ As a member of the quality assurance team (Bioconjugates), you will be responsible to ensure production of API`s is in accordance with Good Manufacturing Practice (GMP).
â?¢ Support the contract manufacturing and advise members of development, production and analytical departments on all aspects of GMP.
â?¢ Responsible for checking manufacturing documentation for conformity, processing of change controls and reviewing and approving of deviations and OOS-results.
â?¢ In addition, you will be the quality contact for our clients, and will present during their GMP audits.
Your background
â?¢ 3-5 years of professional experience in the biopharmaceutical industry, ideally in a GMP area.
â?¢ English language at professional fluency, German language at B1 required for daily interaction with the team (mandatory).
â?¢ Your most recent experience should be in QA.
â?¢ A degree in the Life Sciences (microbiology, biotechnology, chemistry).
â?¢ Experience with TrackWise, SAP, LIMS and DMS is a plus.
â?¢ Strong communication skills, experience in working with stakeholders from different departments.
What's on offer
â?¢ A 7 month contract, with possibility of extension.
â?¢ a great opportunity to develop your career at a leading international biotechnology company.
If this sounds like you, apply below or reach out directly to Hugo Palejowski, recruiter: Write an email.
Contract type: Contract
Start Date: ASAP
Location: Visp
Workload: 100%
Work type: Hybrid
Duration: end of 2024 (possibility of extension)
Your mission
â?¢ As a member of the quality assurance team (Bioconjugates), you will be responsible to ensure production of API`s is in accordance with Good Manufacturing Practice (GMP).
â?¢ Support the contract manufacturing and advise members of development, production and analytical departments on all aspects of GMP.
â?¢ Responsible for checking manufacturing documentation for conformity, processing of change controls and reviewing and approving of deviations and OOS-results.
â?¢ In addition, you will be the quality contact for our clients, and will present during their GMP audits.
Your background
â?¢ 3-5 years of professional experience in the biopharmaceutical industry, ideally in a GMP area.
â?¢ English language at professional fluency, German language at B1 required for daily interaction with the team (mandatory).
â?¢ Your most recent experience should be in QA.
â?¢ A degree in the Life Sciences (microbiology, biotechnology, chemistry).
â?¢ Experience with TrackWise, SAP, LIMS and DMS is a plus.
â?¢ Strong communication skills, experience in working with stakeholders from different departments.
What's on offer
â?¢ A 7 month contract, with possibility of extension.
â?¢ a great opportunity to develop your career at a leading international biotechnology company.
If this sounds like you, apply below or reach out directly to Hugo Palejowski, recruiter: Write an email.
À propos de l'entreprise
