5 of 5 GMP Jobs in the Thames Valley

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 ❯

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 ❯

standards. Your new role As a Quality Assurance Specialist, you will be responsible for managing quality activities to ensure compliance with Good Manufacturing Practices (GMP) and Good Distribution Practices (GDP) for medicinal products. Your key duties will include: Overseeing the product release and compliance process, verifying documentation completeness, and ensuring … field. Minimum of 5 years of experience in Quality Assurance, Quality Control, or a related function within the pharmaceutical or healthcare industry. Certifications in GMP and GDP Strong understanding of regulatory affairs, quality assurance, and pharmaceutical guidelines. Proven experience managing quality systems, pharmaceutical product releases, and compliance-related activities such More ❯

To complete customer line forms, questionnaires and specification requests. To set up and maintain data in the companys ERP system(s). To undertake GMP audits according to agreed audit schedule, distribute the results and ensure the closure of actions raised. To lead and/or participate in root cause … methodical, with excellent administrative and strong communication skills. Good relationship building skills with both internal and external stakeholders. An understanding of the principles of GMP and Global Food Safety Initiatives. Personal Skills An excellent multi-tasker, able to manage multiple projects simultaneously and who thrives in a fast paced role More ❯

/office arrangement as the business requires. The role of the Senior Technical Editor is to manage the creation of new documents and revise GMP documents for complex technical changes. Key responsibilities: Independently manage the creation of new documents and revise GMP documents for complex technical changes according to documented … Tasks and CAPAs Creation and coordination of Change controls and completion of change assessments in Trackwise in conjunction with internal Lonza donors Maintenance of GMP document templates and document style and format standards Advise on document style and content, use of DMS, documentation procedures and documentation best practice and provide More ❯