26 to 50 of 53 GMP Jobs in the UK excluding London

across global pharma accounts, CDMOs, and CGT innovators. Build, manage, and expand multi-stakeholder relationships across Manufacturing, Clinical R&D, production, QA/QC, GMP IT and procurement functions. Develop and execute account-based strategies for Tier 1–3 Pharma, MedTech, CDMOs and CGT manufacturers. Identify whitespace opportunities within existing ...

across global pharma accounts, CDMOs, and CGT innovators. Build, manage, and expand multi-stakeholder relationships across Manufacturing, Clinical R&D, production, QA/QC, GMP IT and procurement functions. Develop and execute account-based strategies for Tier 1–3 Pharma, MedTech, CDMOs and CGT manufacturers. Identify whitespace opportunities within existing ...

across global pharma accounts, CDMOs, and CGT innovators. Build, manage, and expand multi-stakeholder relationships across Manufacturing, Clinical R&D, production, QA/QC, GMP IT and procurement functions. Develop and execute account-based strategies for Tier 1–3 Pharma, MedTech, CDMOs and CGT manufacturers. Identify whitespace opportunities within existing ...

across global pharma accounts, CDMOs, and CGT innovators. Build, manage, and expand multi-stakeholder relationships across Manufacturing, Clinical R&D, production, QA/QC, GMP IT and procurement functions. Develop and execute account-based strategies for Tier 1–3 Pharma, MedTech, CDMOs and CGT manufacturers. Identify whitespace opportunities within existing ...

across global pharma accounts, CDMOs, and CGT innovators. Build, manage, and expand multi-stakeholder relationships across Manufacturing, Clinical R&D, production, QA/QC, GMP IT and procurement functions. Develop and execute account-based strategies for Tier 1–3 Pharma, MedTech, CDMOs and CGT manufacturers. Identify whitespace opportunities within existing ...

across global pharma accounts, CDMOs, and CGT innovators. Build, manage, and expand multi-stakeholder relationships across Manufacturing, Clinical R&D, production, QA/QC, GMP IT and procurement functions. Develop and execute account-based strategies for Tier 1–3 Pharma, MedTech, CDMOs and CGT manufacturers. Identify whitespace opportunities within existing ...

across global pharma accounts, CDMOs, and CGT innovators. Build, manage, and expand multi-stakeholder relationships across Manufacturing, Clinical R&D, production, QA/QC, GMP IT and procurement functions. Develop and execute account-based strategies for Tier 1–3 Pharma, MedTech, CDMOs and CGT manufacturers. Identify whitespace opportunities within existing ...

across global pharma accounts, CDMOs, and CGT innovators. Build, manage, and expand multi-stakeholder relationships across Manufacturing, Clinical R&D, production, QA/QC, GMP IT and procurement functions. Develop and execute account-based strategies for Tier 1–3 Pharma, MedTech, CDMOs and CGT manufacturers. Identify whitespace opportunities within existing ...

across global pharma accounts, CDMOs, and CGT innovators. Build, manage, and expand multi-stakeholder relationships across Manufacturing, Clinical R&D, production, QA/QC, GMP IT and procurement functions. Develop and execute account-based strategies for Tier 1–3 Pharma, MedTech, CDMOs and CGT manufacturers. Identify whitespace opportunities within existing ...

across global pharma accounts, CDMOs, and CGT innovators. Build, manage, and expand multi-stakeholder relationships across Manufacturing, Clinical R&D, production, QA/QC, GMP IT and procurement functions. Develop and execute account-based strategies for Tier 1–3 Pharma, MedTech, CDMOs and CGT manufacturers. Identify whitespace opportunities within existing ...

across global pharma accounts, CDMOs, and CGT innovators. Build, manage, and expand multi-stakeholder relationships across Manufacturing, Clinical R&D, production, QA/QC, GMP IT and procurement functions. Develop and execute account-based strategies for Tier 1–3 Pharma, MedTech, CDMOs and CGT manufacturers. Identify whitespace opportunities within existing ...

across global pharma accounts, CDMOs, and CGT innovators. Build, manage, and expand multi-stakeholder relationships across Manufacturing, Clinical R&D, production, QA/QC, GMP IT and procurement functions. Develop and execute account-based strategies for Tier 1–3 Pharma, MedTech, CDMOs and CGT manufacturers. Identify whitespace opportunities within existing ...

across global pharma accounts, CDMOs, and CGT innovators. Build, manage, and expand multi-stakeholder relationships across Manufacturing, Clinical R&D, production, QA/QC, GMP IT and procurement functions. Develop and execute account-based strategies for Tier 1–3 Pharma, MedTech, CDMOs and CGT manufacturers. Identify whitespace opportunities within existing ...

across global pharma accounts, CDMOs, and CGT innovators. Build, manage, and expand multi-stakeholder relationships across Manufacturing, Clinical R&D, production, QA/QC, GMP IT and procurement functions. Develop and execute account-based strategies for Tier 1–3 Pharma, MedTech, CDMOs and CGT manufacturers. Identify whitespace opportunities within existing ...

will provide strategic leadership for the IFS product roadmap, ensuring its alignment with organisational objectives, timely and high-quality delivery and adherence to GMP compliance standards where needed, playing a key part in advancing our mission and making a real difference. Please note, this is a hybrid opportunity based ...

weekend work (In addition to a normal 37 hour, 5 day shift operation) - Be comfortable working in a highly regulated environment (existing knowledge of GMP practices beneficial but not essential) - Have experience using Microsoft Office suite - Have an analytical mind with acute attention to detail - Have good problem-solving abilities ...

monitor standards, provide coaching where needed, and escalate any risks to ensure corrective actions are taken promptly. Key Responsibilities Carry out process audits including GMP, fabrication, foreign body, CCP, glass & hard plastic audits Verify and audit production paperwork for accuracy and completion Coach and support production staff to ensure correct ...

monitor standards, provide coaching where needed, and escalate any risks to ensure corrective actions are taken promptly. Key Responsibilities Carry out process audits including GMP, fabrication, foreign body, CCP, glass & hard plastic audits Verify and audit production paperwork for accuracy and completion Coach and support production staff to ensure correct ...

monitor standards, provide coaching where needed, and escalate any risks to ensure corrective actions are taken promptly. Key Responsibilities Carry out process audits including GMP, fabrication, foreign body, CCP, glass & hard plastic audits Verify and audit production paperwork for accuracy and completion Coach and support production staff to ensure correct ...

collected for testing schedules and testing schedules are met Logging micro samples Accurate carrying out of positive release checks for all finished products GMP audits/Glass and plastic audits, including generation of improvement areas, completing database Ensure close outs of non-conformances Sampling and recording of finished product shelf ...

completed Collecting micro samples as per schedule Traceability Investigations into complaints Daily auditing of CCPs Daily label checks Calibration Auditing of processing records GMP/Fabric audits Temperature checks Quality checks The nature of the role requires a flexible approach to working hours. Core working hours are: Nights: Monday ...

Data Consulting Manager - must have GMP expertise A growing data and digital consultancy is looking for an experienced Digital Consulting Manager to join its London-based team. This role is ideal for someone who enjoys leading complex client projects, building trusted senior relationships, and developing high-performing teams. The Role ...

typing skills Must be willing to work overtime and flexible shifts as required Essential Knowledge, Skills, and Abilities •Follows all safety, USDA, and GMP policies and guidelines. •Maintain a clean and organized work area. •Ability to work in a fast-paced environment. •Ability to communicate effectively and follow verbal ...

Responsibilities •Perform varying manual, repetitive tasks to process meat from the turkeys. •Ensure product safety and product defense in the plant. •Follows all GMP and HACCP procedures that relate to product safety with the facility. •Supports all Food Safety initiatives. •Some tasks are performed using tools or equipment, while others ...

Some knowledge of Unix-based operating systems, use of the command line and SQL is advantageous • Strong knowledge of Contracting Out Requirements such as GMP• Strong Defined Benefit Knowledge, including historical knowledge of UK Pensions Legislation. Due to the volume of applications received for positions, it will not be possible ...