15 of 15 GMP Jobs in the South East

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 ❯

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 ❯

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 ❯

investigations. What We’re Looking For: 5+ years of experience in Site Reliability Engineering or a related field. Hands-on experience with Biosafety and GMP environments. Strong foundation in Lean Six Sigma principles. Proven problem-solving skills with a knack for performance tuning. Effective communicator and team player. Formal education More ❯

investigations. What We’re Looking For: 5+ years of experience in Site Reliability Engineering or a related field. Hands-on experience with Biosafety and GMP environments. Strong foundation in Lean Six Sigma principles. Proven problem-solving skills with a knack for performance tuning. Effective communicator and team player. Formal education 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 ❯

As a technician, you'll follow precise mechanical CAD drawings to assemble, perform testing (including force and measurement), inspect assemblies, and document processes to GMP standards. Experience working in safety-critical industries (e.g., medical, aerospace, or automotive) is a plus. Key Responsibilities: Interpret and follow mechanical CAD drawings (SolidWorks preferred More ❯

DMPs, CDPs, ad servers, and programmatic advertising. • Proficiency in AI/ML applications for ad targeting, personalization, and optimization. • Experience with Google Marketing Platform (GMP), Amazon Ads, The Trade Desk, or similar ecosystems. • Strong understanding of cloud architectures (AWS, Azure, GCP) and big data technologies. • Experience with privacy-first advertising More ❯

and take ownership of site-wide quality processes, with particular focus on data integrity, validation oversight, documentation, and continuous improvement of systems that support GMP/GDP operations. You’ll also work closely with colleagues across Quality, Validation, Manufacturing, and IT, providing compliance guidance and driving a strong quality culture. … to Quality leadership team projects and initiatives to enhance overall site compliance Ideal Experience: Extensive experience in pharmaceutical QA, with a strong understanding of GMP and GDP Proven track record in managing QMS elements, including validation, documentation, and data integrity Experience supporting inspections and audits, both internal and external Excellent 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 ❯

projects in accordance with the company project roadmap throughout the project lifecycle ensuring governance to current engineering standards and compliance with CDM regulations. Strict GMP compliance to be adhered throughout the lifecycle of the project. Coordination with the Principal Contractor and all other project team members to ensure completion to … budget and provide accurate monthly reports Attendance at daily update meetings Ensure compliance with all HSE & CDM requirements Ensuring compliance of project delivery with GMP requirements and company UKSL SOP’s Develop and updated project schedule defined appropriately according to project stage-gate Identify, record and monitor project risks, seeking … level Project Engineer/Project Manager with experience in managing cross functional teams, delivering complex Manufacturing Facility and processing projects, in a highly automated GMP production environment Demonstrated capacity to effectively manage and execute projects from initiation to completion Full project lifecycle experience from end to end design through to More ❯

projects in accordance with the company project roadmap throughout the project lifecycle ensuring governance to current engineering standards and compliance with CDM regulations. Strict GMP compliance to be adhered throughout the lifecycle of the project. Coordination with the Principal Contractor and all other project team members to ensure completion to … budget and provide accurate monthly reports Attendance at daily update meetings Ensure compliance with all HSE & CDM requirements Ensuring compliance of project delivery with GMP requirements and company UKSL SOP’s Develop and updated project schedule defined appropriately according to project stage-gate Identify, record and monitor project risks, seeking … level Project Engineer/Project Manager with experience in managing cross functional teams, delivering complex Manufacturing Facility and processing projects, in a highly automated GMP production environment Demonstrated capacity to effectively manage and execute projects from initiation to completion Full project lifecycle experience from end to end design through to 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 ❯

the Works. - Delivery of a portfolio of small to medium-sized projects, ensuring governance to current engineering standards and compliance with CDM regulations. - Strict GMP compliance throughout the project lifecycle. - Coordination with the Principal Contractor and project team members to ensure completion on schedule. - Oversee completion snags and construction defects. … and work elements. - Manage stakeholder expectations. - Monitor project budget and provide monthly reports. - Attend daily update meetings. - Ensure compliance with HSE & CDM requirements and GMP standards. - Develop and update project schedules. - Identify and monitor project risks. - Resource planning and communication of resource needs. - Other duties relevant to the role of … project engineer. Qualifications - Degree in a relevant science/engineering discipline. - Experience managing cross-functional teams and delivering complex manufacturing projects in a GMP environment. - Full project lifecycle experience from design to C&Q and handover. - Knowledge of project management processes. - Excellent communication and organizational skills. - Proven track record of More ❯