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QA Associate – Laboratory
role focused on GMP quality oversight for the QC lab in Geel, with strong emphasis on
deviations, investigations, CAPAs, data integrity, and release support .
Role overview
Support QC laboratory activities from a
quality assurance
perspective.
Ensure laboratory work stays compliant with
cGMP
and internal procedures.
Help secure
timely and reliable release of test results .
Act as a bridge between
laboratory, production, and quality
teams.
Main responsibilities
Perform QA oversight of
QC laboratory operations .
Do
QA walk-throughs / check rounds
in lab areas.
Review and approve
SOPs, work instructions, protocols, validation documents, and reports .
Handle and follow up on
Change Controls, Deviations, OOS/OOTs, and CAPAs .
Review investigations, root cause analyses, and corrective actions.
Track quality records to ensure proper closure and effectiveness.
Support trending and identify recurring lab issues.
Contribute to small improvement projects and quality initiatives.
Key requirements
Degree in
Chemistry, Pharmaceutical Sciences, Life Sciences, Bioengineering, or similar .
Experience in
QA, QC, or laboratory operations
in a GMP pharmaceutical environment.
Deviation handling is mandatory .
Strong knowledge of
cGMP, ICH guidelines, and data integrity .
Good understanding of
laboratory testing, qualification/validation, release, and distribution processes .
Strong analytical thinking and risk-based decision making. xlxgzvr
Able to work independently and communicate well across teams.
Candidate fit in one line
Best suited to someone with a
strong GMP QC/QA background, especially someone who has handled
lab deviations, investigations, CAPAs, and documentation review .
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