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Grafton Recruitment

Quality Documentation Specialist (GMP, Pharma) - QC Laboratory

Grafton Recruitment Show all offers
Łódź
Expires Nov 4, 2026
28 days ago

In short

Quality Documentation Specialist needed in Łódź for a pharma/biopharma company. Responsibilities include developing and verifying GMP documentation, preparing procedures, supporting audits, and collaborating with labs. Requires higher education in biotech/pharma, GMP experience, English (B1), and analytical skills.

Keywords

GMP quality control pharmaceutical industry biopharmaceutical industry documentation laboratory analysis analytical methods validation

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Published 2026-10-05
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