Position: Entry level

Job type: Full-time

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About The RoleThis role is responsible for sample management in a biotech manufacturing environment. Serving as a technical specialist in the QC space, this person will be expected to act independently and have a strong overall understanding of QC functions and regulationsResponsibilities
  • Prepare and review QC documentation including SOPs & CAPAs
  • Responsible for QC sample management
  • Identify gaps in processes and systems according to cGMP
  • Proficient using various Quality systems as well as LIMS
  • Document and perform sample-related non-conformance investigations
  • Support internal and regulatory audits
Requirements
  • BSc in a Life Sciences subject
  • Minimum 2 years’ relevant work experience in a biotech/pharma/medical device environment
  • Good understanding of industry regulations and guidelines
  • Good knowledge of Quality systems including LIMS
  • Experience managing and authoring QC documentation
  • Able to accommodate a shift structure including weekend and evenings
  • Fluent English and Dutch language
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Deadline: 19-12-2025

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