1 to 25 of 76 Permanent GMP Jobs in England

management on future actions. Ensure audits are carried out such that assurance is provided for all vendors/suppliers in accordance with current EU GMP, EU GDP or equivalent, and the relevant marketing authorisation (MA) Monitor and maintain CAPAs (both internally and with external suppliers) Responsible for maintaining vendor validity More ❯

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 ❯

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 ❯

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 ❯

and process transfer expected to exceed 5 years. Prior experience with biopharmaceutical product registration preferably with FDA and/or EMEA. Knowledge of current GMP's, ICH Guidelines, and FDA/EU validation practices for biopharmaceutical processes required. Preferred Qualifications: If you have the following characteristics, it would be a More ❯

of PQS IT systems like Veeva Vault. Experience with documentation management Top 3 must have skills Documentation writing skills Communication/collaboration Understanding of GMP compliance Description: Enrolment and site maintenance of the global standards process. Support with the documentation management processes. Support with implementation of the global systems incl. More ❯

technology development and process transfer expected to exceed 5 years.Prior experience with biopharmaceutical product registration preferably with FDA and/or EMEA.Knowledge of current GMP's, ICH Guidelines and FDA/EU validation practices for biopharmaceutical processes required. Preferred Qualifications: If you have the following characteristics, it would be a More ❯

and process transfer expected to exceed 5 years. Prior experience with biopharmaceutical product registration preferably with FDA and/or EMEA. Knowledge of current GMP's, ICH Guidelines and FDA/EU validation practices for biopharmaceutical processes required. Preferred Qualifications: If you have the following characteristics, it would be a 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 ❯

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 ❯

to deliver concise documentation and adapt writing style to audience as appropriate. Educated to degree level or higher. Understanding of EU & UK GDP/GMP legislation. QUALIFICATION, EXPERIENCE & SKILLS DESIRABLE Experience in multiple regulatory and operational jurisdictions. 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 ❯

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 ❯

apply.\n\nPlease contact Mark Bux-Ryan for further details.\n\nKey experience:\n\n * Experienced within a pharmaceutical QA position, working in a GMP environment. Ideally upwards of 5 years.\n\n * Experience of sterile manufacturing is an advantage, but not essential\n\n * A desire to manage a 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 ❯

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 ❯

are met Tracking and managing project fees Managing projects related to new business activities Providing project management support for various client projects, such as GMP projects, buy-ins/outs, investment changes, and digital initiatives Managing business change projects and system development/enhancement projects, liaising with IT and third More ❯