VRS UK is seeking a GMP QA professional to manage and uphold the QMS as it aims for GMP accreditation. You will audit readiness across departments, conduct self-inspections, and train teams in best practices to support a fast-growing rural Wiltshire operation.
Key responsibilities include maintaining the QMS, handling deviations, CAPAs, and change controls, and contributing to health and safety compliance. A proactive, detail-oriented approach with strong communication is essential.
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GMP QA Specialist: QMS & Audit Leadership employer: VRS-UK
Join a leading pharmaceutical company that prioritises innovation and employee development in the heart of the bioprocessing industry. With a collaborative work culture, you will have access to cutting-edge technology and hands-on experience in upstream process development, while benefiting from opportunities for career growth and professional advancement. This role not only offers a chance to contribute to groundbreaking biologics but also fosters a supportive environment where your contributions are valued and recognised.
