1 to 25 of 31 GMP Jobs in the UK excluding London

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 ...

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 ...

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 ...

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 ...

customer compliance. Maintaining nutritional information and recipe data within internal systems. Supporting customer, third-party and BRCGS audits. Conducting internal audits and supporting GMP compliance activities. Participating in HACCP, TACCP and VACCP activities, including vulnerability assessments. Monitoring food safety alerts, emerging legislation and industry developments. Investigating specification, labelling and customer ...

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 ...

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). ...

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 ...

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 ...

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 ...

rotation, with particular focus on short shelf-life products such as poultry. Complete the monthly audit schedule, including: Brittles Audit, Document Check Audit, Full GMP Audit Carry out weekly internal audits and other scheduled compliance checks, escalating any issues or concerns promptly to management. Conduct traceability and mass balance exercises … directed by management. Undertake any other reasonable duties as requested by the line manager. QA Manager Skills & Competencies Strong knowledge of food safety, HACCP, GMP, and quality management systems Excellent attention to detail and organisational skills & Strong problem-solving and investigative ability Effective communication and leadership skills & Ability to prioritise ...

will translate complex processes and investigations into structured, easy-to-follow documentation. This role is critical to ensuring operations remain inspection-ready and GMP/GDP compliant . This is a factory-based role , with time spent both on the production floor and in a dedicated computing/documentation area. … SMEs) to ensure accuracy and relevance Support document updates in line with process changes, audits, and system improvements Compliance & Governance Ensure all documents meet GMP and GDP standards , including version control and traceability Identify gaps or risks in documentation and drive improvements Maintain documentation aligned with site Quality and document ...

Specialist will play a key role in supporting site validation activities across a range of projects. This is a great opportunity for someone with GMP validation experience looking to build on their existing knowledge within a supportive and expanding team. Candidates with equipment or process validation experience from pharmaceutical … other GMP-regulated manufacturing environments are encouraged to apply. The role: Plan and execute validation activities in line with site validation plans and project timelines. Author and maintain validation protocols and reports across multiple validation areas such as: Cleaning validation Computerised systems validation Equipment and utilities qualification Process validation Interpret ...

secondary packaging and labelling activities and support the QP with release activities. Provide guidance and support on GDP and GMP compliance to ensure product quality is not compromised Provide Guidance and Support on Good Documentation Practice and Data Integrity to ensure GxP records are generated and retained appropriately Carry … risk assessments on business, GDP and GMP critical areas and has experience in conducting risk assessments Provide backup support in case of other quality members absence Conduct Quality tasks as requested by the line manager in support of business activities Position Requirements To be successful in this role you must ...

promoting a positive food safety and quality culture Maintain and improve the Quality Management System in line with BRCGS and customer requirements Manage HACCP, GMP, pest control, hygiene, and product testing programmes Conduct internal audits and support external audits and customer visits Investigate non-conformances and customer complaints, implementing corrective … years' experience within a Quality role, including team leadership responsibilities HACCP Level 3 qualification (minimum) Internal auditing experience Strong knowledge of food safety, GMP, hygiene, and pest control programmes Experience working within BRCGS accredited environments desirable Milling or food manufacturing experience advantageous Strong communication, organisation, and people management skills Ability ...