Operating within a virtual pharmaceutical model, the company works closely with Contract Manufacturing Organisations (CMOs), providing broad exposure to external manufacturing and quality assurance activities. This role offers a hybrid working pattern and the opportunity to develop within a collaborative and supportive Quality team.
You will be responsible for:
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Reviewing batch manufacturing and packaging records to ensure compliance with GMP requirements prior to product release.
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Performing batch release activities, ensuring products meet the required quality standards before distribution.
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Working closely with external manufacturing partners and internal stakeholders to support day-to-day quality assurance activities.
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Maintaining accurate quality documentation while supporting compliance with GMP and the Quality Management System.
The successful candidate will have:
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Previous Quality Assurance experience within a GMP-regulated pharmaceutical, biotechnology or medical device environment.
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Experience reviewing batch records and/or supporting batch release activities.
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A strong understanding of GMP principles and pharmaceutical quality systems.
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Excellent attention to detail, communication skills and the ability to work effectively with both internal teams and external manufacturing partners.
Quality Assurance | QA | Quality Assurance Officer | GMP | Good Manufacturing Practice | Batch Record Review | Batch Release | QMS | Quality Management System | Pharmaceutical | Medical Devices | CMO | Contract Manufacturing Organisation | Compliance | GDP | Hybrid
Salary description
£30000.00 - £35000.00 per year
