Allerton Bishop is proud to be searching on behalf of a market leader in pharmaceutical manufacturing to appoint a Qualified Person (QP). This is a strategic role to shape quality assurance in the clients UK manufacturing site, while supporting the release of life changing pharmaceutical products. As a Qualified Person (QP), you will take a pivotal role in maintaining product integrity and regulatory compliance across a complex site. Reporting to the Quality Director, you will drive continuous improvement across all aspects of GMP compliance and batch release.
Key Responsibilities:
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Act as Releasing QP for pharmaceutical products under MHRA license.
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Ensure compliance with GMP, UK regulations, and corporate/global quality procedures.
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Oversee batch certification, deviation handling, CAPA management, and investigations.
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Support site readiness and performance during MHRA inspections.
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As the Qualified Person (QP), you will act as a coach and mentor to Quality Assurance and Quality Control teams.
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Support the Director of Quality to improve and update the Global Quality Management System.
Candidate Requirements:
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Eligibility to be named as a Qualified Person (QP) on a UK manufacturing license.
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Quality Assurance work experience within a UK-licensed pharmaceutical environment.
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Track record of releasing medicinal products as a Qualified Person (QP).
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Experience of all product dosage forms will be considered.
Quality Assurance | QP | Qualified Person | Pharmaceutical | Oral Solid Dose | Inhalation | Sterile | Aseptic | Biopharmaceutical | Biologics | ATMPs | Cell Therapy | Gene Therapy.