26 to 39 of 39 Permanent GMP Jobs

through the QMS. Conduct audit trail reviews. · Perform area walkthroughs to identify and resolve non-compliance. Audit raw data, protocols and validation reports for GMP compliance. Maintain and promote audit readiness. Ensure protocols and validation reports are approved according to project schedules. Lead process audits and support GMP audit activities. … Local Quality Councils and project meetings. Provide QA SME support for Operations, QC, MSAT and Development Services. Mentor and coach business partners in GMP practices. Advise scientists on documentation and follow-up expectations. Provide out-of-hours QA support where required. Act as a GMP SME enforcing site quality processes. ...

impact digital transformation projects in the Pharmaceutical industry? This opportunity offers the chance to work on cutting-edge MES implementations and validation strategies within GMP-regulated environments in the UK. Due to upcoming project needs, we are looking for a Senior Consultant – MES & Validation (Siemens Opcenter Execution Pharma … Opcenter Execution Pharma Contribute to the definition of Validation Master Plans and overall validation strategy Review and assess validation documentation to ensure compliance with GMP requirements and project standards Evaluate the system integrator’s project methodology and assess the quality and consistency of deliverables Ensure alignment with project expectations, regulatory ...

food safety, legality and quality standards across site operations Audit, maintain and challenge HACCP systems and prerequisite programmes Carry out internal audits including GMP, hygiene, glass & plastic and quality management systems Support and prepare for customer, retailer and third-party audits including BRCGS and IFS standards Manage non-conformances, investigations … experience within a QA or Technical role in Food Manufacturing Experience supervising or leading teams within a food manufacturing environment Strong understanding of HACCP, GMP, food safety and quality systems Experience supporting customer, retailer and third-party audits Knowledge of corrective actions, root cause analysis and non-conformance management Strong ...

Automation & CSV Engineer (Permanent) - West Yorkshire Pharmaceutical Manufacturing High-Tech GMP Environment Career Growth Opportunity An exciting opportunity is available for an Automation & Computer System Validation (CSV) Engineer to join a highly regulated manufacturing environment within the pharmaceutical/life sciences sector. This role is ideal for an engineer … maintain automation and control systems across manufacturing operations Troubleshoot equipment and process-related automation issues Participate in computerized system validation (CSV) activities within a GMP-regulated environment Assist with qualification, commissioning, and lifecycle management of automated systems Support continuous improvement and process optimization projects Collaborate with engineering, production, quality ...

quality, and regulatory compliance. You will be responsible for maintaining high quality and compliance standards across the business, ensuring all products meet regulatory and GMP requirements. Sector – Pharmaceutical Manufacturing Non-Negotiable Requirements of the QA Officer Previous QA experience Experience working within a pharmaceutical or regulated environment Requirements … background Experience supporting regulatory submissions Knowledge of batch record review and product quality reviews Experience working with Quality Management Systems (QMS) Strong understanding of GMP and regulatory standards (MHRA, ISO) Experience with documentation control and SOP writing Ability to manage deviations, CAPAs, and change controls Strong attention to detail ...

product investigations Coordinate and resolve immediate/urgent customer complaints, ensuring prompt responses/resolution Participate in the internal audit programme to ensure continued GMP compliance of all site activities Utilise scientific resources in order to work on improving quality of products and services To maintain personal training folder … Controls CAPAs Deviations Complaints Recalls OOS/OOT The Person: Will have a Degree in a relevant- Scientific discipline Will have good knowledge of GMP Experience in CAPA, Deviations, OOS, OOT, Internal auditing (preferred), Customer Complaints handling would be very advantageous Strong IT skills (Microsoft applications) Good interpersonal skills ...

product investigations Coordinate and resolve immediate/urgent customer complaints, ensuring prompt responses/resolution Participate in the internal audit programme to ensure continued GMP compliance of all site activities Utilise scientific resources in order to work on improving quality of products and services To maintain personal training folder … Controls CAPAs Deviations Complaints Recalls OOS/OOT The Person: Will have a Degree in a relevant- Scientific discipline Will have good knowledge of GMP Experience in CAPA, Deviations, OOS, OOT, Internal auditing (preferred), Customer Complaints handling would be very advantageous Strong IT skills (Microsoft applications) Good interpersonal skills ...

environment. This role will focus on SAP Extended Warehouse Management design, testing and delivery , with a strong requirement for candidates who have worked in GMP-regulated environments . Key Responsibilities Lead and support SAP EWM design workshops Translate warehouse, quality and compliance requirements into functional designs Support SAP EWM configuration … activities Work closely with Warehouse, Quality, Manufacturing, Validation and IT teams Support SIT, UAT, defect resolution and process alignment Ensure EWM processes align with GMP, GxP, validation and audit requirements Produce and maintain functional specifications, test scripts and validation evidence Required Skills & Experience Proven experience as an SAP EWM Consultant ...

supplier approval, including SAQs, audits, and certification requirements • Support and lead raw material elements of internal, customer, and group audits • Audit compliance with QMS, GMP, and HACCP standards, driving corrective actions to closure • Monitor KPIs, identify trends, and drive continuous improvement initiatives • Communicate customer and business requirements clearly to suppliers … ensure compliance and robustness • Ability to work cross-functionally with Technical, Operations, NPD, and suppliers • Strong audit capability with a clear understanding of GMP and HACCP requirements • Highly organised with excellent attention to detail • Strong communication skills, able to influence at all levels • Proactive mindset with the ability to anticipate ...

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 ...

will be joining a global biopharmaceutical organisation with a strong presence across oncology, rare diseases, and neuroscience, and a well-established footprint in GMP manufacturing. The business is recognised for its commitment to innovation, advanced therapies, and high-quality production standards, alongside a growing focus on digital transformation and operational … digital initiatives.You will be responsible for managing projects, supporting manufacturing systems (e.g. MES, LIMS, automation), and ensuring all systems operate in line with GMP and data integrity requirements. This is a highly visible position with strong interaction with site leadership and cross-functional teams. What you'll need to succeed ...