Position: Associate

Job type: Full-time

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Due to the substantial increase in our business, we are currently looking for a Quality Assurance Specialist, to join our team of consultants.

Your tasks:

  • Within the quality operations department, the Quality Assurance Expert assures that all operations meet or exceed cGMP regulations ensuring the quality of Drug Substance
  • Responsible for root cause analysis and corrective action for product and process-related deviation / non-conformances related to the biotech production
  • Responsible for quality operations including Change Control review, Batch records review, review/audit of data and reports as specified by Standard Operating Procedures

Your profile:

  • Bachelor’s degree or Master’s degree is needed, preferably in a scientific topic (Pharmacy, Chemistry, Biology, Biotechnology, etc.)
  • At least 1 year of experience in Quality Assurance/Quality Operations in the pharmaceutical or biotech industry
  • Excellent knowledge of regulatory requirements, including GMP guidelines
  • Previous experience with systems like Trackwise, MES
  • Excellent knowledge of English
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Deadline: 13-05-2024

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