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This role will take full ownership of site quality, leading a small team of QA and QC staff. The main responsibilities will be ensuring site GMP compliance, as well as being primary point of contact for customer and regulatory authorities.
Client Details
Our client is a manufacturer of unlicences medicines (specials) as well as IMP products in varying dosage forms for both human and veterinary markets.
This business operates a variety of markets, including NHS, Retail, Contract Manufacturing and Export, and so are expected to meet a variety of quality standards and legislative requirements.
Description
- Lead the Quality team, completing regular training, mentoring, anc coaching.
- Develop and implement a quality improvement agenda to drive continious improvement programme.
- Ensuring all licensing and accrediation necessary to operate are maintained.
- Act as point of contact for Customer and Regulatory authorities.
- Appoint quality resource as appropriate to uphold regulatory compliance
Profile
- Subject Matter Expert in GMP compliance
- Knowledgable on IMPs and Specials
- Strong people leader
- QP and/or RP is preferrable
Job Offer
- Strong basic salary, with good package.
- Opportunity to develop a career within a growing business.
- Hybrid working
