1 to 25 of 45 GMP Jobs in the UK

supply chain landscape. Stakeholders & Vendors: Coordinate with corporate IT, regional business teams, 3PLs, and vendors. Compliance: Manage OT/IT convergence while ensuring GMP, food safety, and cybersecurity compliance. Must-Have Qualifications Experience: 10-15 years in IT with a strong focus on supply chain and FMCG manufacturing. Critical Migration ...

data validation and reconciliation at every phase - scope, transformation, load and extended business health checks post-migration Ensuring full compliance with GDPR, data privacy, GMP, food safety and information security regulations throughout. What You Must Bring 8-12 years of hands-on experience in IT data management with a clear ...

party audits or visits, including corrective or preventive action close-outs Stay up to date of current technical information in food manufacturing Monitor GMP, Glass & Plastic standards and complete inspections Drive factory hygiene and quality standards Maintain and review the HACCP, TACCP and VACCP plans Lead the Food Safety ...

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 ...

conformance is properly managed and closed in a timely manner. Ensure Company HACCP Plans are up to date, relevant and implemented effectively. Ensure GMP procedures, as according to company policies, are being always adhered to. Ensure the raw material and finished product testing programme is maintained and performed as according ...

relevant managers. Conduct daily spot checks on stock rotation, particularly for short-coded items. Complete monthly auditing schedules, including brittles, document checks, and full GMP audits. Perform weekly internal audits and scheduled checks, promptly reporting concerns to management. Conduct traceability and mass balance checks in line with the Quality Management ...

user computing, shop floor systems, manufacturing execution systems (MES), laboratory systems, and site-based applications. Ensure compliance with regulatory and quality standards (e.g., GMP, GxP, data integrity, cybersecurity requirements) across all supported sites. Lead and coordinate site IT teams and regional resources, fostering a strong service culture aligned with business ...

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 ...

data and presenting insights Regulatory & Compliance Knowledge (Critical in LIMS) Understanding of: GxP (Good Practice standards) FDA 21 CFR Part 11 ISO 17025/GMP Knowledge of: Electronic signatures Audit trails Data validation processes Infrastructure & Environment Skills Windows Server environments Deployment models On-premise and cloud-hosted LIMS Security concepts ...

LIMS, LabWare implementations or laboratory informatics platf orms.Knowledge of laboratory operations, sample lifecycle management and scientific workf lows.Familiarity with Computer Systems Validation (CSV), GxP, GMP, GLP, ISO standards or data integrity princi ples.Experience delivering projects involving system integrations, laboratory instruments, ERP systems, APIs or cloud-hosted applicat ions.Formal project management ...

timeframes. Experience Proficient experience using DeltaVTM at configuration and software test level. Experience in other forms of software testing is advantageous. Familiarity with GAMP5, GMP, good documentation practices and regulatory requirements for automated systems e.g., ISO9001, 21CFR Part11. Experience working within the biotechnology, pharmaceutical or medical device industry. Education Bachelor ...

activities (IQ/OQ/PQ) for equipment and processes Ensure timely delivery of KPIs and departmental objectives The Person Proven experience within a GMP-regulated environment in a similar QA/Validation role Experience in equipment validations (writing reports), the ideal applicant will have process validation experience too Previous ...

responsible for overseeing multiple cross-functional initiatives, including Manufacturing Execution Systems (MES), automation, data integrity, and regulatory compliance programs, ensuring alignment with business objectives, GMP standards, and global IT strategies. The ideal candidate will bring a strong background in program management, combined with extensive knowledge of pharmaceutical manufacturing systems, regulatory ...

Manager Previous experience working as a QA Manager or Senior QA professional within food manufacturing. Strong knowledge of BRCGS standards, HACCP, GMP, and food safety systems. Experience leading quality and hygiene teams within a manufacturing environment. Hands-on experience managing audits, non-conformances, and customer complaints. Desirable Requirements ...

embedding Greencore, customer, and legal standards, ensuring compliance is consistently achieved and maintained. This role plays a critical part in driving improvements in GMP performance and audit readiness, helping to raise quality standards and strengthen food safety culture across the site. Role Accountabilities Understand and apply Greencore, customer ...

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 ...

laboratory environment and/or software development environment. Experience integrating instruments via serial/USB/Ethernet connections. Knowledge of Oracle databases. Understanding of GMP, GAMP or regulated software validation. Experience delivering customer training. Full UK driving licence. What we offer Career development and professional growth opportunities. Competitive salary. ...

with routine QMS activities such as document reviews, training record tracking, and audit readiness Skills & Experience Required Experience working within a regulated environment (e.g. GMP, pharmaceutical, or life sciences) Strong attention to detail with a focus on documentation accuracy and data integrity Experience using document management systems (e.g. Veeva, TrackWise ...

/radio compliance) is highly valued Nice to have: experience with structured validation approaches (IQ/OQ/PQ), regulated environments (GDP/GMP), or frameworks such as CFR 21 Part 11 Comfortable working in a small, distributed team, with a willingness to travel occasionally, domestically and internationally, for testing ...

products and processes meet the highest regulatory and quality standards. What youll do: Evaluate Manufacturing and Quality processes for compliance with ISO 13485, GMP, and FDA 21 CFR 820. Support Quality, Manufacturing and cross-functional teams with investigations, documentation, and continuous improvement. Support continuous improvement to manufacturing process through NCRs … audits. Review/approve SOPs and product/equipment specifications. Adhere to Quality Management System (QMS) requirements in line with Corins Good Manufacturing Practice (GMP) as per ISO13485 & FDA21 CFR Part 820. Work with multiple stakeholders internally; R&D, Operations and Validation plus many others. Analyse quality data, support product ...

standard. • Supporting investigations relating to raw material, packaging and supplier quality concerns. • Assisting with supplier audits, customer audits and site visits when required. • Ensuring GMP, HACCP, Food Safety and Health & Safety standards are maintained at all times. • Supporting continuous improvement activities across the Technical and Quality functions. • Providing technical support ...

Experience with LIMS platforms such as Clinisys WinPath, LabVantage, STARLIMS, LabWare, or equivalent. Familiarity with validation, UAT, and regulated environments (ISO 15189, ISO 13485, GMP, GxP) is advantageous. ...

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 ...

operations, ensuring consistent QA oversight across both sites Drive robust HACCP implementation, including real-time CCP verification and immediate escalation of any deviations Oversee GMP, hygiene, and environmental monitoring programmes to maintain high site standards Manage incident escalation, investigations, and non-conformance processes to ensure timely resolution Ensure full compliance ...