7 of 7 Permanent GMP Jobs in London

Life Science, Pharma, Biotech, or MedTech sectors. Deep understanding of R&D, clinical trials, manufacturing, or regulatory frameworks. Familiarity with MHRA, HPRA, EMA, FDA, GMP, GCP, GLP, ISO 9001, ISO 13485. Experience delivering technology-enabled, engineering-led, or data-driven solutions into regulated environments. Strong commercial awareness with understanding ...

Carry out organoleptic and quality testing as required. Audits & Compliance Conduct daily and weekly internal audits, including: Glass and hard plastic audits Hygiene audits GMP inspections Investigate non-conformances and complete root cause analysis reports. Support external audits and calibration activities. Assist with supplier approval processes and documentation reviews. Liaise ...

product direction across cross‐functional, multi-region teams. A strategic thinker capable of shaping long-term transformation while executing fast. Comfortable in complex, regulated, GMP-heavy environments. Experience delivering solutions that optimise manufacturing performance, supply chain planning, network strategy, quality workflows, data governance & AI compliance. Why This Role Matters This ...

Minimum of five years' experience in Quality Assurance within food manufacturing, ingredient distribution, or a related FMCG environment. Strong working knowledge of BRCGS, HACCP, GMP, CAPA management, and root cause analysis techniques including FMEA, 5 Whys, and Fishbone. Proven experience conducting supplier audits, managing customer complaints, investigating non-conformances ...

performance Manage relationships with third-party IT vendors, internal IT teams, and data governance stakeholders Lead data-focused activities such as actuarial valuation extracts, GMP equalisation, and pension dashboards Ensure compliance with UK pension legislation, reporting requirements, and governance standards Analyse large datasets, improving data quality, validation processes, and reporting ...

primary liaison between manufacturing sites, IT, Quality, and business stakeholders, ensuring successful delivery of PAS-X migration activities while maintaining compliance within a regulated GMP environment. Key Responsibilities Own and maintain the PAS-X re-hosting project plan, ensuring alignment with the wider Digital Manufacturing programme roadmap and migration strategy. … regular updates to programme leadership and steering committees. Lead third-party vendors, system integrators, and infrastructure partners throughout the project lifecycle. Ensure compliance with GMP, GxP, CSV and regulatory requirements. Required Experience Proven experience delive ring Körber PAS-X (Werum P AS-X) projects within pharmaceutical or life sciences environments. ...

safety standards in line with Greencore, customer, and legal requirements, with guidance from the QA Supervisor or Manager. Role Accountabilities • Audit compliance with QMS, GMP, and HACCP, raising clear non-conformances and driving corrective actions to closure • Apply an inquisitive audit mindset to identify root causes and reduce repeat … actions • Work safely at all times, promoting strong health, safety, and environmental standards What we're looking for • A strong understanding of quality systems, GMP, HACCP, and traceability within a manufacturing environment • A proactive, detail-focused approach with a natural curiosity to challenge and improve standards • Confidence working hands ...