Allerton Bishop are currently supporting a pharmaceutical business in its search for a QP to join its quality team in the Midlands. This is an opportunity to play an important role in product quality and patient safety, working closely with manufacturing, quality control and the wider business.
The role
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Certify and release batches in accordance with the relevant manufacturing authorisation, GMP requirements and product approvals.
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Review batch documentation and ensure deviations, investigations and relevant quality issues are appropriately resolved before certification.
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Provide QP input on sterile manufacturing activities, including contamination control and aseptic processing.
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Support investigations, CAPAs, change controls and ongoing improvements to the quality management system.
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Work with quality, manufacturing and technical teams to maintain inspection readiness and support regulatory inspections.
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Provide quality oversight and guidance to colleagues, contributing to a strong quality culture.
The right candidate
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Eligible to act as a Qualified Person in the UK, with experience of batch certification.
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Experience in a GMP-regulated pharmaceutical manufacturing environment, with a focus on sterile products.
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Good knowledge of aseptic processing, contamination control and relevant GMP requirements, including EU GMP Annex 1.
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Experience reviewing batch records and managing deviations, investigations and change controls.
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Confident working across teams and making sound, independent quality decisions.
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Able to work on site in the Midlands 4 days per week.
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