26 to 47 of 47 GMP Jobs in the UK

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 ...

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). ...

enhance LabWare LIMS applications to ensure optimal performance and reliability. Support system upgrades, testing, validation and deployment activities within regulated environments (GxP/GMP). Collaborate with laboratory, quality and IT stakeholders to drive process improvements and ensure compliance with regulatory requirements. ...

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 ...

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 ...

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. ...

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 ...

logistics partners to ensure their systems and processes are aligned to programme timelines and go-live readiness. Ensure all system changes are compliant with GMP, food safety, and relevant regulatory requirements - particularly in plant and operational environments. About You Important: this role is designed for someone whose career started … testing, and cutover design. Familiarity with master data governance (MDG) and data migration approaches - including data profiling, cleansing, cutover validation, and reconciliation. Experience with GMP, food safety compliance, or equivalent regulated manufacturing frameworks as they relate to IT system changes. Randstad Technologies is acting as an Employment Business in relation ...

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 ...

client, a growing pharmaceutical organisation, is seeking a Quality Systems Officer to join their Quality team. This is an excellent opportunity for someone with GMP experience looking to develop their career within Quality Assurance and Quality Systems. Key Responsibilities: Supporting the day-to-day maintenance of the Quality Management System … Assessments Assisting with internal audits and audit readiness activities Supporting customer complaints, investigations and quality records management Maintaining training records and ensuring compliance with GMP requirements Participating in continuous improvement initiatives across the business Experience Required: Degree qualified in a Scientific discipline (preferred) Previous GMP experience within Pharmaceutical, Biotechnology ...

more than a "keep the line running" position, it's heavily involved in automation, system setup, validation and continuous improvement within a GMP-regulated setting. The Role You'll play a key role in delivering and supporting automated manufacturing systems across the site, working closely with engineering, projects and operations … platforms Leading and supporting capital projects from concept through to validation Developing technical documentation including SOPs, specifications and validation protocols Supporting GMP compliance, change control and validation activities (IQ/OQ/PQ) Troubleshooting and resolving process control and automation issues Supporting new product and technology introduction from an engineering ...

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 ...

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 ...

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 ...

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 ...

Business Development Executive Full time, permanent Worcester Office based 30,000 + commission Job Purpose GMP Recruitment are proud to be partnering with a well-established and growing organisation who is seeking an experienced Business Development Executive. The Business Development Executive is responsible for identifying new business opportunities, building … negotiation and influencing abilities. Ability to build rapport and maintain professional relationships at all levels. Self-motivated with a proactive and results-driven approach GMP Recruitment Agency Ltd are recruiting for this role on behalf of their client and are acting as an employment agency. ...