7 of 7 Permanent GMP Jobs in the East of England

a scientific discipline (e.g., microbiology, biology, biomedical sciences) or equivalent. Proven experience in quality assurance within a regulated manufacturing or laboratory environment. Strong knowledge of quality systems, ISO standards, GMP/GDP principles, and regulatory compliance. Skilled in leading audits, managing CAPAs, and interpreting quality metrics. Excellent leadership, communication, and problem-solving abilities. Proficient in data analysis tools, LIMS, and More ❯

A minimum of ten years' experience leading IT at a senior management level Track record of delivering results quickly Experience in delivering IT services to customers Work in a GMP or highly regulated environment Preferred Experience: Experience of agile product development Experience of Lean Six Sigma Infrastructure delivery (networking, hardware) to customers Experience with data science project delivery Knowledge/ More ❯

looking for a QA Manager to join their Technical team. In this QA Manager position you will lead the QA team and be responsible for delivering high levels of GMP, food safety and integrity standards within the factory. You will also be responsible for updating and maintaining the QMS, conduct audits and ensure any corrective actions are implemented. As the More ❯

act as point of contact for the Archives facility (Archives Champion) for documentation queries. This will include preservation notices management, capacity monitoring, destruction management and liaison for archive documentation GMP queries. Qualifications & experience: · SVQ Level 3: Highers/higher national certificate/apprenticeship or equivalent More ❯

the functioning of the QMS, providing oversight to key stakeholders alike (including senior staff members). Accountability across (but not limited to); change control, stability, documentation control, internal audits, GMP, supplier approval, complaints, PQRs, NPI, route cause analysis and controlled drug returns. Ensuring compliance/correct documentation practices, i.e batch records, laboratory tests and quality agreements too. Overseeing supplier verification … batch review process. Keeping abreast of evolving UK & EU retained regulations (for the purposes of pharmaceutical and/or food/ingredients manufacturing). To ensure compliance with EU GMP standards & BRC food safety requirements. Managing the preparation process (and heavily involved in hosting activities) for MHRA inspections, customer (third party audits) and acting as the lead person. Enrsuring quality … bodies. Deputising for the HOQ when required. The Person:- The ideal Candidate will hold a degree in a STEM related subject Experience managing QA team/s in an GMP/Pharmaceutical setting. Management experience essential (will consider Team Leader or similar). Experienced in batch review and batch release Experience in auditing and audit hosting Experience in CAPA, deviations More ❯

Site Name: UK - Hertfordshire - Ware RD Posted Date: Oct We are looking for an experienced and motivated engineer with an expertise in modelling to support the development of complex combination products. This role offers the chance to deliver innovative, patient More ❯

act as point of contact for the Archives facility (Archives Champion) for documentation queries. This will include preservation notices management, capacity monitoring, destruction management and liaison for archive documentation GMP queries. Qualifications & experience: SVQ Level 3: Highers/higher national certificate/apprenticeship or equivalent Experience with Veeva Vault Experience with GMP environments More ❯