Location: Beerse (On-site)
...
quality associate – laboratory compliance & data review.
- posted 2 days ago
- closes 20 october 2026
key responsibilities
- Data Review & Data Integrity: Perform independent reviews of analytical data packages (e.g., release, stability, method validation) to ensure accuracy, data integrity, and GMP compliance. Identify inconsistencies or risks, and escalate findings where necessary.
- Inspection Readiness: Conduct readiness checks and ensure all required documentation is complete, available, and up to date.
- Compliance & QA Support: Assist in executing QA check rounds and monitoring compliance activities across various laboratories.
- Process Alignment: Contribute to core compliance processes (such as sample management, training procedures, and non-conformance handling) in strict accordance with defined standards.
- Advisory & Coaching: Guide and support laboratory teams on data integrity standards, documentation best practices, and GMP expectations.
- Continuous Improvement: Actively support initiatives aimed at optimizing compliance workflows and data review methodologies.
qualifications
- Education: Master’s degree in a scientific discipline (e.g., Bioengineering, Pharmaceutical Sciences, Chemistry, Biochemistry, or equivalent).
- Experience: Relevant experience working within a GMP-regulated pharmaceutical laboratory environment.
- Knowledge: Sound understanding of GMP guidelines and data integrity principles.
- Skills: Strong analytical thinking, problem-solving capabilities, and a risk-assessment mindset.
- Communication: Excellent written and verbal communication skills.
- Collaboration: A true team player comfortable working effectively alongside lab teams, compliance units, and Quality Assurance in a diverse, cross-functional setting.
- Organization: Proactive mindset, strong planning capabilities, and the ability to manage strict deadlines.
- Languages: Fluent in English (spoken and written).
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