Quality Assurance

il y a 4 semaines


Ghent, Belgique Vivid Resourcing Temps plein

Location: Ghent, Belgium Company: Global leader in production for biomedical, pharmaceutical, food, and technical industries Salary: Up to €7,000 + Premium Belgium Package My client are seeking a Quality Assurance & Validation Specialist to help ensure that all biomedical products are manufactured, packaged, stored, and distributed in full compliance with current Good Manufacturing Practices (cGMPs). You'll join a collaborative team and report to the Quality and Compliance Manager Biomedical to uphold quality and drive improvements across our operations. AREA OF RESPONSIBILITY AND RELATED TASKS: • Quality Assurance · Disposition of finished product batches & preparation of certificates of analysis · Incoming release of materials and packaging components · Investigation and resolution of non-conformances, deviations, and complaints · Approval of change controls and supplier qualifications · Management of specifications, QMS documentation and training program · Performing internal audits · Support during customer and authority audits, including CAPA follow-up · Documentation support towards customers • Validation · Development of validation masterplans, protocols (IQ/OQ/PQ) and related documentation · Execution of validation tests and coordination with external partners · Oversight of process validation activities and QC results · Ownership of re-qualifications and centralized validation archive · Contribution to risk assessments (FMEA) PROFILE · 2+ years of experience in the (bio)pharmaceutical industry with working knowledge of GMP (EU & US)· Skilled in root cause analysis and structured problem-solving · Strong communicator with the ability to influence and collaborate across teams · Proficient in Dutch and English Organized, detail-oriented, and proactive WE OFFER THE OPPORTUNITY AND CHALLENGE · Impact: Your expertise will directly shape product quality and validation, fueling innovation in life sciences. · Growth in a Global Leader: Be part of an international organization recognized for its pioneering role for biomedical applications. · Learning That Lasts: Expand your skill set in GMP compliance, Quality Management Systems and validation technologies in a supportive environment. If the role sounds interesting and you feel you have the necessary experience please do get in touch with me: trishan.patel@vividresourcing.com 033180074



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