26 to 38 of 38 GMP Jobs

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 ...

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 ...

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 ...

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 ...

regulated pharmaceutical setting. The role will focus on Emerson DeltaV systems, supporting configuration, integration, and lifecycle delivery of control systems, while ensuring compliance with GMP and data integrity standards. You will work closely with multidisciplinary teams to develop and review key automation documentation, support testing activities, and contribute to system … mechanical, and electrical teams to ensure seamless system delivery Assisting with FAT activities and coordinating with vendors and project stakeholders Ensuring automation activities meet GMP expectations and data integrity standards (e.g. ALCOA+) Taking part in design reviews, HAZOP studies, and risk assessment workshops Managing updates to design documentation through change ...