1 to 25 of 39 GMP Jobs in England

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

process and the implementation of the ISA S-88 standard Working knowledge of software maintenance in a regulated environment (preference for work experience with GMP, GAMP in a biopharmaceutical or pharmaceutical environment) Ability to perform administrative tasks in automation systems (E.g., DeltaV, PI, Infobatch). ...

integration Experience with Oracle and/or PostgreSQL databases Understanding of laboratory workflows and Laboratory Information Management Systems Experience working within regulated environments (GxP, GMP, ISO 17025 or FDA 21 CFR Part 11) Desirable Experience with both SampleManager v12.1 and v21.3 Oracle to PostgreSQL migration experience Previous public sector ...

essential. Previous QA experience in the management of (CAPA, Deviation, Change Controls, Complaints, PQRs, Management Reviews, recalls, Strong knowledge of: Good Manufacturing Practice (GMP) and GxP EU Annex 11 21 CFR Part 11 GAMP 5 Data integrity principles and MHRA expectations Experience supporting or leading regulatory inspections and audits Required ...

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. ...

Quality oversight across all Manufacturing, QC, Engineering and supporting operational areas. This includes Quality support for projects, initiatives, and routine activities associated with all GMP operations on site. They lead a team that delivers 24/7 QA coverage to Primary and Secondary manufacturing, ensuring continuous quality presence and timely … site operations, and to contribute effectively to the strategic development of company systems. Directly responsible for ensuring implementation and use of Quality Systems for GMP areas in the facility, such as DR/CAPA management, Change Management, document management and training systems. Locally, the QP (if eligible) must provide oversight ...

whilst maintaining strong relationships Act as HACCP Team Leader for the Glycosade facility and pilot plant, ensuring robust food safety systems and compliance Drive GMP excellence through auditing, ensuring compliance, identifying opportunities for improvement and delivering timely closure of corrective actions. Manage site quality assurance programmes, ensuring effective oversight … frequent travel and at short notice when required Proven experience in leading, motivating and developing a team Strong knowledge of Quality Management Systems (QMS), GMP, HACCP and FSSC 22000 requirements. Experience leading quality investigations and root cause analysis Experience managing customer complaints, adverse events , non-conformances and quality assurance processes ...