6 of 6 GMP Jobs in the South East

across global pharma accounts, CDMOs, and CGT innovators. Build, manage, and expand multi-stakeholder relationships across Manufacturing, Clinical R&D, production, QA/QC, GMP IT, and procurement functions. Develop and execute account-based strategies for Tier 1–3 Pharma, MedTech, CDMOs and CGT manufacturers. Engage and build relationships with ...

Quality Assurance Officer (GMP/Cannabinoids) Sandwich Up to £40,000 + Company Bonus + Private Healthcare + Pension + Training Are you a Quality Assurance Officer or similar with GMP experience looking to join an innovative pharmaceutical manufacturer operating within one of the fastest-growing areas of the life … continued growth of a business operating in an exciting and evolving sector. This role would suit a Quality Assurance Officer or similar with GMP experience looking to broaden their technical expertise within a specialist pharmaceutical environment, where they'll have genuine responsibility, opportunities to influence quality systems and excellent prospects ...

experienced Technical Writer with a background in GMP-regulated manufacturing? Do you have a talent for turning complex technical processes into clear, compliant documentation? If so, this Technical Writer could be perfect for you. This Technical Writer is an onsite opportunity based in Petersfield click apply for full job details ...

this role would be: Reviewing and approving deviations, CAPAs and change controls within defined timelines. Supporting manufacturing teams as a QA partner to ensure GMP compliance during production activities. Reviewing batch documentation and support preparation for Qualified Person batch disposition. Participating in investigations, root cause analysis and risk assessments … quality events. Reviewing and approving SOPs, protocols, reports and other GMP documentation. Supporting implementation of new manufacturing processes for incoming client programs. Contributing to continuous improvement initiatives to strengthen quality systems and operational processes. We are looking for: Experience in a GMP-regulated pharmaceutical, biotechnology or similar manufacturing environment. Significant ...

candidate will act as a technical leader for manufacturing systems, process optimisation, equipment performance, and implementation of new technologies while ensuring full compliance with GMP, quality system, and regulatory requirements. Key Responsibilities: Team Leadership & Development: Lead, mentor, and develop a team of Automation Engineers and Continuous Improvement (CI) Engineers … quality, maintenance, and process data to identify trends and improvement opportunities. Quality, Compliance & Regulatory Support: Ensure all engineering activities are performed in accordance with: GMP requirements, ISO 13485 requirements, FDA Quality System Regulations, Internal quality procedures. Cross Functional Collaboration: Work closely with Operations, Quality, Validation, Maintenance, Supply Chain, Regulatory ...

secondary packaging and labelling activities and support the QP with release activities. Provide guidance and support on GDP and GMP compliance to ensure product quality is not compromised Provide Guidance and Support on Good Documentation Practice and Data Integrity to ensure GxP records are generated and retained appropriately Carry … risk assessments on business, GDP and GMP critical areas and has experience in conducting risk assessments Provide backup support in case of other quality members absence Conduct Quality tasks as requested by the line manager in support of business activities Position Requirements To be successful in this role you must ...