QA Associate

Sector: PharmaceuticalsReference: BBBH189347_1793199058Join a Growing Life Science Leader! About the OpportunityAre you experienced in reviewing quality or batch documentation in a regulated environment? This expanding life science organisation is seeking a committed Quality Assurance Associate to support their Quality Assurance function and ensure documentation excellence across the business.

This role is also suitable for people with a strong Quality or data review background in food and drink or the medical device and similarly regulated industries. Reporting to the Quality Assurance Manager, you will play a critical role in maintaining compliant, accurate, and well controlled documents, data, and records.

Key ResponsibilitiesReview quality and batch documentation with accuracy and attention to detailProvide document control functions, support, and guidance across the businessMaintain trackers and generate accurate status reports to support batch compilation activitiesSupport document archiving, ensuring controlled and compliant material movementCoordinate SOP review cycles and ensure revisions meet required timelinesEnsure all documents are updated, mastered, and maintained according to established proceduresContribute to GMP compliance activities and continuous QA improvementRequirementsHNC/HND minimum; degree preferredExperience in document review within a regulated GMP environment is preferred but they will consider people from an ISO 9001 or ISO13485 background.

Strong written and verbal communication skills at all levelsKnowledge of Quality Systems (desirable)Excellent organisational skills, with the ability to work independently and as part of a teamAnalytical approach to problem solving and decision makingProficiency in Microsoft Office and confident data entry skillsGuidant, Carbon60, Lorien & SRG - The Vertage Group Portfolio are acting as an Employment Business in relation to this vacancy.

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