Qualified Person (QP)

Walker Cole International is supporting a leading pharmaceutical manufacturing organisation in the search for a Qualified Person (QP) to join their growing team within the UK. This is an excellent opportunity for an experienced QP to join a fast-paced manufacturing facility supporting the release of specialist pharmaceutical products.

Do you have the right skills and experience for this role Read on to find out, and make your application.

Your Responsibilities as the Qualified Person

• Certify and release GMP batches in line with relevant regulatory requirements and marketing authorisations.
• Support and oversee Quality Management System activities, ensuring ongoing GMP compliance.
• Provide quality leadership across manufacturing, deviations, change controls and client interactions.
• Act as a key quality representative during internal, client and regulatory audits and inspections.
• Support continuous improvement initiatives across quality and manufacturing operations.
• Review and approve quality documentation including investigations, CAPAs and risk assessments.
• Collaborate with cross-functional teams to ensure compliance across production and supply chain activities.

The Successful Candidate

• Eligible to act as a Qualified Person under permanent provisions with relevant scientific degree qualifications.
• Previous experience acting as a named QP on a manufacturing licence within a GMP environment.
• Strong understanding of batch certification, GMP compliance and pharmaceutical quality systems.
• Confident stakeholder management skills with the ability to work cross-functionally across technical and operational teams.
• Proven ability to manage competing priorities within a fast-paced GMP manufacturing environment. xwzovoh
• Strong communication skills with a proactive and quality-driven approach.

Qualified Person | QP | Batch Release | GMP | Quality Assurance | QA | QMS | EU GMP | Annex 16 | MHRA | Batch Certification | Pharmaceutical Manufacturing | Regulatory Compliance | Change Control | Deviations | CAPA | Audit | Pharmaceutical Quality | CDMO | Product Release

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