QA Associate (m/f) 100%

nemensis ag

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QA Associate (m/f) 100%

We support our client, an international biopharmaceutical company specialized in immuno-oncology, in the search for a one year position in their northwest location.

Your responsibilities:

  • To review and archive quality documents (batch records, manufacturing and packaging master documents, analytical data, etc.) and record data into databases
  • To proactively identify and communicate any deficiencies in documents (deviations, OOS, etc.)
  • To support on corrective measures and during the implementation of the global specification onto the local site
  • To collaborate in the preparation of quality internal and external inspections
  • To participate in the preparation of GMP trainings

Your profile:

  • Completed laboratory technician training or BSc in Chemistry, Biochemistry, Biology or Pharmacy
  • At least 1-2 years experience in a laboratory, manufacturing or documentation in a pharmaceutical company
  • Experience working with GMP regulations and FDA requirements
  • Good written and spoken English and German
  • Good knowledge of MS Office and SAP

What the company offers you in return:

  • Work in an international environment
  • 40 hours/week
  • Location easily reachable with own car and public transportation

Welcome to nemensis!

We are looking forward to getting to know you.