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Product Compliance Specialist

Job Reference: FJ-3fmtr

Manufacturing and Production
Folkestone, Kent
Discussed upon application
Temporary

Product Compliance Specialist

(GMP / QA)

Type: Temporary

Location: Folkestone

Working hours: Mon-Thurs 08:00-16:30, Fri 08:00-15:30 (30 mins unpaid lunch daily)

Pay: DOE (Depending on Experience)

Hands-on QA Operations role in regulated manufacturing, supporting medical devices and cosmetics at a busy Folkestone site.

About the role

Quality and compliance depend on strong GMP oversight at every stage. In this hands-on position, you'll work across manufacturing and goods-in to ensure materials, documentation, and release decisions meet approved standards-helping drive a proactive quality culture on the shop floor and in the warehouse.

Key responsibilities

    • Promote and embed GMP and a proactive quality culture across QA and Production.
    • Carry out QA activities supporting the manufacture and distribution of medical devices and cosmetics.
    • Inspect, sample and evaluate incoming components/packaging against approved specifications.
    • Review, approve and release components and packaging materials in SAP (Systems, Applications and Products).
    • Review batch records, manage discrepancies, and support batch/finished product release.
    • Manage deviations, non-conformances and CAPAs (Corrective and Preventive Actions) via the Agile system, ensuring timely closure.
    • Maintain compliant TQM (Total Quality Management)/GMP documentation and controlled records.
    • Maintain reference samples and controlled artwork libraries; provide Certificates of Analysis (CoA) as required.
    • Provide QA oversight at goods-in (including rejection labelling) and resolve issues cross-functionally.

Skills & experience

Essential

    • Strong attention to detail and confident decision-making using data and evidence.
    • Good IT skills (MS Word/Excel) and comfortable working with quality systems.
    • Able to plan ahead, use initiative and respond positively to change.

Desirable

    • QA experience within a regulated industry (FMCG, medical devices, pharma, cosmetics).
    • Science/engineering-based education.
    • Knowledge of ISO 22716 and/or ISO 13485.

Health & Safety & culture

Safety is a top priority; you must follow all site H&S procedures and report accidents/near misses.

All applicants will be assessed solely on suitability, without regard to age, gender, disability, ethnicity, religion, belief, or sexual orientation.

How to apply

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