1 to 25 of 53 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 ❯

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 ❯

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 ❯

hear from you. Full training on internal quality processes is provided to the successful candidate. Role 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 ❯

hear from you. Full training on internal quality processes is provided to the successful candidate. Role 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 ❯

for IT Compliance Assessments, Inspections Readiness and Support. Also, it is important to cover key information about Regulatory Inspections and differences in terms of GMP, GLP, and GCP. Properly coordinate internal assessments including scope, schedule, and assessors. Access Management: Actively contribute to the development of the Access Management Program, related More ❯

or similarregulated sectors with a Total Quality Management approach. - Experience in the application and management of Quality Management Systems to meet ISO 13485 and GMP requirements. - Ability to implement company systems, processes and policies with consistency, being a key presence on site championing quality assurance and quality improvement initiatives within 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 ❯

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 ❯

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 ❯

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 ❯

providing excellent service to clients and third parties with a desire to succeed at accomplishing challenging objectives. Desirable Criteria Knowledge of and experience with GMP Reconciliation/Equalisation calculations. Practical knowledge of the Pension Protection Fund (PPF). Circumstances Working hours: Monday to Friday, 37.5 hours per week with additional More ❯

continually enhance our relationships with key platform partners. Working to ensure we deliver against agreed JBPs with all key partners. Including Google, SA360/GMP & Microsoft. Team Leadership & Operational Excellence Being a visible role model to PPC Account Directors and Senior Account Managers. Demonstrating a proactive, highly positive/mature More ❯

Engineering, or a similar subject. Extensive industry experience in validation, engineering, or operations within a cGMP environment. A working knowledge and practical experience with GMP utilities, equipment, DIA, and CSV. Key Words: Senior Validation Engineer/Biotech/Validation/cGMP/CQV/DIA/CSV/Qualification Protocols More ❯

a similar MEP-focused role, ideally within Data Centres, Pharmaceutical, or Cleanroom environments Previous experience delivering projects for hyperscale or co-location data centres, GMP/pharma clients, or other critical infrastructure is highly desirable Knowledge of commissioning protocols, integrated systems testing (IST), and regulatory compliance in regulated environments Proficient More ❯

such as Controls & Instrumentation 2. Proven calibration experience working in a highly regulated manufacturing environment, such as Pharmaceutical, Food, Beverage or Chemical. Ideally to GMP standards. 3. A working knowledge and practical experience with PLC, SCADA, and HMI systems. Ideally Allen Bradley or Siemens. More ❯