Overview
Please read the information in this job post thoroughly to understand exactly what is expected of potential candidates.
This is a 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.
Responsibilities
Perform QA oversight of QC laboratory operations.
Conduct QA walk-throughs and 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.
Qualifications and 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.
Able to work independently and communicate well across teams. xlxgzvr
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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