QA Specialist – Commissioning

New Opportunity: QA Specialist – Commissioning & Qualification (C&Q) Ensuring high-level compliance and robust qualification processes is critical to delivering safe, reliable therapies and healthcare solutions. We are currently recruiting a QA Specialist
- C&Q to act as a key quality partner across system lifecycle and qualification projects. Your role:
- Lifecycle & Qualification Oversight: Review and approve critical qualification packages, including URS, risk assessments, DQ/IQ/OQ/PQ protocols, test scripts, and summary reports.
- Compliance & Procedures: Review and approve procedures tied to system qualification, calibration, maintenance, and lifecycle management.
- Quality Investigations: Assess and thoroughly investigate deviations related to system qualification, maintenance, or usage, defining effective CAPAs.
- Audit Readiness: Serve as a subject matter expert for C&Q topics during internal audits, client visits, and regulatory inspections.
- Cross-Functional Collaboration: Challenge constructively and work closely with engineering, validation, and operations teams to meet project deadlines. What we are looking for:
- Medior QA profile with hands-on experience in a strictly regulated environment (Pharma/Biotech).
- Solid background in qualification (C&Q / CQV) deliverables and QA methodologies.
- Rigorous compliance mindset paired with constructive communication skills.
- Ability to manage multiple priorities and maintain strong relationships with stakeholders. Interested in this challenge? Reach out via direct message or share your resume at hanna.mimouni@randstad.be to explore the opportunity. #QualityAssurance #QA #CommissioningAndQualification #Validation #GMP #BiotechJobs #PharmaRecruitment