11 of 11 Permanent GMP Jobs in the South East

and embedded analytics for production KPIs. Exposure to SAP IBP, PP/DS, or advanced scheduling tools is highly desirable. Awareness of industry manufacturing standards and regulatory compliance frameworks (GMP, ISO, etc.). Stakeholder & Soft Skills Strong engagement skills with manufacturing stakeholders: Heads of Production, Plant Managers, and COOs. Ability to translate complex operational processes into streamlined SAP-enabled solutions. More ❯

Participate in Technical audits including customer and Group Technical, ensuring all relevant raw material information is available and completed in the required timescale Audit compliance against Quality Management Systems, GMP and HACCP controls, raising all non-conformances against relevant standards with objective evidence, effectively communicated to enable the operational teams to take the appropriate and necessary corrective action & to follow More ❯

Participate in Technical audits including customer and Group Technical, ensuring all relevant raw material information is available and completed in the required timescale Audit compliance against Quality Management Systems, GMP and HACCP controls, raising all non-conformances against relevant standards with objective evidence, effectively communicated to enable the operational teams to take the appropriate and necessary corrective action & to follow More ❯

checks, supplier and internal non-conformance, customer complaint investigations, glass & plastic audits, and fabrication audits. - Supporting the training of staff and verification against CCPs, policies and procedures. - Conducting internal GMP audits across departments and conducting hygiene verifications. - Assisting with external audits. The role will be a mix of factory and office-based work to meet the needs of the business More ❯

applications and embedded analytics for shop floor and KPI reporting. Advantageous: exposure to IBP, PP/DS, or advanced scheduling tools. Awareness of manufacturing standards and compliance (e.g., ISO, GMP). Soft Skills & Leadership Strong communication and stakeholder management, particularly with operations, production, and executive-level teams. Ability to translate complex business processes into practical SAP-based solutions. Confident presenting More ❯

follow-up, and root cause 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 in an engineering-related discipline. More ❯

follow-up, and root cause 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 in an engineering-related discipline. More ❯

patient outcomes. About the Role We're hiring a QA Compliance Manager to lead a team focused on maintaining and enhancing the Quality Management System (QMS) in compliance with GMP, ISO 9001, ISO 13485, and other regulatory standards. Reporting to the Head of Quality, you'll oversee internal audits, batch record reviews, CAPA systems, and customer audits, while also supporting … opportunity with potential Qualified Person (QP) sponsorship for the right candidate. Key Responsibilities: Lead and develop the QA Compliance team Maintain and improve the QMS in line with EU GMP and ISO standards Oversee internal audits, CAPA management, and batch documentation review Host customer audits and support regulatory inspections Drive continuous improvement and contribute to strategic quality initiatives Support training … change control, and compliance projects Candidate Requirements Essential: Degree in a scientific discipline (e.g. Chemistry, Biology, or related field) 10+ years' experience in GMP-regulated environments Strong leadership and people management skills In-depth knowledge of EU cGMP, ISO 9001, and ISO 13485 Experience supporting or conducting batch release under QP supervision Lead Auditor training and a proactive approach to More ❯

transform, and cleanse member data Design and implement tools and processes to resolve client data issues Review and quality-check the technical work of others Support projects such as GMP reconciliation, rectification exercises, and data audits Manage multiple projects simultaneously, ensuring delivery on time and within scope About You Strong knowledge of DB pensions administration systems and their data structures More ❯

the functioning of the QMS, providing oversight to key stakeholders alike (including senior staff members). Accountability across (but not limited to); change control, stability, documentation control, internal audits, GMP, supplier approval, complaints, PQRs, NPI, route cause analysis and controlled drug returns. Ensuring compliance/correct documentation practices, i.e batch records, laboratory tests and quality agreements too. Overseeing supplier verification … batch review process. Keeping abreast of evolving UK & EU retained regulations (for the purposes of pharmaceutical and/or food/ingredients manufacturing). To ensure compliance with EU GMP standards & BRC food safety requirements. Managing the preparation process (and heavily involved in hosting activities) for MHRA inspections, customer (third party audits) and acting as the lead person. Enrsuring quality … bodies. Deputising for the HOQ when required. The Person:- The ideal Candidate will hold a degree in a STEM related subject Experience managing QA team/s in an GMP/Pharmaceutical setting. Management experience essential (will consider Team Leader or similar). Experienced in batch review and batch release Experience in auditing and audit hosting Experience in CAPA, deviations More ❯

with health authorities, contract manufacturers, and internal stakeholders to ensure compliance across the product lifecycle. Key Responsibilities Lead product release and compliance activities, ensuring documentation accuracy and adherence to GMP/GDP standards. Maintain and improve Quality Systems including Change Control, Deviations, Complaints, Product Quality Reviews (PQRs), Recalls, and Returns. Act as a key liaison with Health Authorities, ensuring timely … Pharmaceutical Sciences, Chemistry, Biotechnology, Biochemistry, or a related discipline. 5+ years' experience in Quality Assurance, Quality Control, or a similar function within the pharmaceutical or healthcare sector. Certifications in GMP and GDP. Strong knowledge of regulatory affairs, pharmaceutical guidelines, and quality systems. Proven experience in compliance activities including CAPAs, Change Control, and Deviations. Exposure to regulatory audits and interactions with More ❯