1 to 25 of 61 Permanent GMP Jobs in the UK excluding London

be provided. Proven experience in leading complex MES projects from concept to deployment. Knowledge and understanding of Pharma and Biotech industry & processes. Familiarity with GMP, FDA 21 CFR Part 11, GAMP5, and other relevant regulatory requirements. Excellent problem-solving, communication, and interpersonal skills. Ability to travel as required to client More ❯

experience leading IT at a senior management level Track record of delivering results quickly Experience in delivering IT services to customers Work in a GMP or highly regulated environment Preferred Experience: Experience of agile product development Experience of Lean Six Sigma Infrastructure delivery (networking, hardware) to customers Experience with data More ❯

implementing IT PQS systems (particularly Veeva Vault) Documentation management expertise Essential Skills Excellent documentation writing capabilities Strong communication and collaboration skills Deep understanding of GMP compliance requirements Project management expertise Ability to manage ambiguity and drive results Detail-oriented with strong organizational skills Collaborative team player with stakeholder management abilities More ❯

implementing IT PQS systems (particularly Veeva Vault) Documentation management expertise Essential Skills Excellent documentation writing capabilities Strong communication and collaboration skills Deep understanding of GMP compliance requirements Project management expertise Ability to manage ambiguity and drive results Detail-oriented with strong organizational skills Collaborative team player with stakeholder management abilities More ❯

and provide sound judgment is highly desired. Understanding of the NPI (New Product Introduction) process and Process Validation is preferred. A thorough understanding of GMP/ISO regulations and validation regulations is preferred. Strong mentoring, coaching and leadership skills are required. Demonstrated project management and project leadership abilities. Rewards & Benefits More ❯

and provide sound judgment is highly desired. Understanding of the NPI (New Product Introduction) process and Process Validation is preferred. A thorough understanding of GMP/ISO regulations and validation regulations is preferred. Strong mentoring, coaching and leadership skills are required. Demonstrated project management and project leadership abilities. Rewards & Benefits More ❯

our grocery retailer partners. Full training on internal quality processes is provided to the successful candidate. Accountabilities: To audit compliance against Quality Management Systems, GMP and HACCP controls, raising all non-conformances against relevant standards with objective evidence. Effectively communicating to enable the operational teams to take the appropriate and More ❯

our grocery retailer partners. Full training on internal quality processes is provided to the successful candidate. Accountabilities: To audit compliance against Quality Management Systems, GMP and HACCP controls, raising all non-conformances against relevant standards with objective evidence. Effectively communicating to enable the operational teams to take the appropriate and More ❯

business. Conducting supplier audits, internal inspections, and management reviews. Key Requirements: Proven experience in a GMDP or similar regulated environment. Strong knowledge of GDP, GMP, ISO 9001, and ISO 13485 standards. Excellent organizational, communication, and stakeholder management skills. A positive attitude toward promoting quality across all departments. Proficiency in MS More ❯

related to CSV to improve inhouse CSV process by identifying areas for enhancement and implementing best practices. Must possess understanding of GCP, GLP, and GMP principles and procedures. Must possess excellent verbal and written communication skills. Proficient in MS Word and other Office applications. A strong team player with the More ❯

related to CSV to improve inhouse CSV process by identifying areas for enhancement and implementing best practices. Must possess understanding of GCP, GLP, and GMP principles and procedures. Must possess excellent verbal and written communication skills. Proficient in MS Word and other Office applications. A strong team player with the More ❯

Wonderware, Ignition) Experience implementing detailed control system electrical design packages Working knowledge of control system networks (Ethernet, ControlNet, DeviceNet, etc.) Understanding of Biopharmaceutical processes, GMP and validation Knowledge of S88 Batch standards and experience implementing batch systems Excellent written and verbal communication skills A DNA comprised of collaboration and teamwork More ❯

teams technical capabilities. To hit the ground and make an immediate impact, we expect MDEs to have a broad understanding of Good Manufacturing Practices (GMP) and a desire to continually improve. Your day-to-day responsibilities: Prepare feedback on Design for Manufacture to Product Design and New Product Launch teams More ❯

enhance digital and data processes to optimize plant operations. Improve procedures relevant to the OSD Engineering Department. About You: Experience working within highly regulated (GMP) environments. Strong numeracy and literacy skills, with a willingness to learn and excellent communication skills. Process safety awareness and risk management experience. Ability to manage More ❯

change management interventions/tactics based on feedback and inputs from project and business stakeholders. Observes and supports all safety guidelines and regulations. Follows GMP and regulatory requirements, and ensures quality standards are met. Models the Company Mission, Vision and Values Statements, policies, and current standard business practices. Performs other More ❯

Strong experience with purchasing high volumes of beef, poultry, pork, and other protein products Understanding of regulatory requirements and food safety standards (CFIA, HACCP, GMP, etc.) Strong network of supplier contacts in the protein industry is an asset Solid understanding of commodity, food and/or packaging sourcing is an More ❯

are 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 More ❯

handling. Working hours:4 days on, 4 days off. Hours based on business and production requirements. Pay: £29,092 per annum Main Responsibilities Conduct GMP audits with production and address any issues. Verify traceability documents have been completed correctly and challenge any mistakes Log complaints and Foreign Bodies conduct investigations More ❯

manufacturing environment. Strong leadership and people management skills. In-depth knowledge of QA processes (QC experience desirable but not essential). Familiarity with ISO, GMP, or similar standards. Excellent communication, organisation, and problem-solving skills. Ability to manage multiple tasks and priorities in a fast-paced setting. What's on More ❯

staff. Liaise with production and technical teams to resolve quality issues in real-time. Contribute to continuous improvement initiatives and compliance with HACCP and GMP standards. The Candidate The successful QA Supervisor is someone who is both proactive and detail-driven, with excellent communication skills and a strong grasp of More ❯

stakeholder management and influence skills at site and wider business levels. Experience in Project Management, especially major technical or capital projects. Thorough knowledge of GMP and Regulatory requirements. Experience using data to drive decision-making. Experience with Quality by Design, FMEA, RCA, and technical risk assessments. Preferred Qualifications and Experience More ❯

and influence stakeholder at site and the wider business Experience of Project Management, particularly major technical and/or capital projects Thorough knowledge of GMP and Regulatory requirements Experience in use of data to drive tactical and strategic decision making Experience of Quality by Design and risk management approaches, including More ❯

FT View SE, FT Batch). Knowledge of Batch Process Control, ISA-S88 standard programming. Knowledge of GAMP, 21 CFR Part 11, ASTM E2500, GMP, etc Knowledge of Virtualisation technology. What We Offer: Comprehensive mindfulness programs with a premium membership to Calm Volunteer Paid Time off available after 6 months More ❯

manufacturing sites. Ensure all assigned project work is delivered on time, on budget, and meets the stage gates and success criteria (including FMEA, DQVV, GMP, and HSE compliance). Support Quality/compliance activities on assigned complaint investigations, RCA, and change management. With guidance from more senior members of the More ❯

to 100% of the time and lifting heavy weights. Knowledge and experience using computer software including ERP system. and possibly Experience in a GMP environment would be advantageous. Certified to handle and ship Dangerous Goods or willingness and ability to be trained immediately. Supplier account management. Working with couriers, customs More ❯