10 of 10 Permanent GMP Jobs in the South East

degree with 8 years of experience; OR a high school diploma (or equivalent) and 10 years of relevant experience working in Quality Assurance, GMP manufacturing environment, pharmaceutical environment, or medical device space Experience supporting quality activities in medical devices, combination products, pharmaceuticals, or another highly regulated industry. Working knowledge ...

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 ...

biotechnology and/or pharmaceutical industry, including senior Quality leadership roles in regulated manufacturing environments. Strong knowledge of global regulatory authorities including FDA, GMP, GCP and GLP requirements. Proven expertise in Quality Management Systems (QMS), with a particular focus on GMP compliance and data integrity. Demonstrated experience with regulatory inspections ...

Pepto-Bismol, and Seven Seas. We are seeking a Qualified Person (QP)/Senior Quality Assurance Manager to lead quality and compliance activities across GMP, GDP and HACCP for food supplements and help safeguard consumer trust across our UK Personal Health Care portfolio. If you thrive at the intersection … accordance with UK legislation for Medicinal Products for Human Use, ensuring batch certification, release, and maintenance of the certification register. Ensure robust GMP, GDP, and HACCP compliance through effective documentation systems, quality and technical agreements, vendor qualification and auditing, and alignment with Marketing Authorisations and Global Healthcare procedures. Lead quality ...

team in Maidstone, Kent. You will bring your experience in leading and contributing to the Design, delivery, compliance and lifecycle management of GMP-compliant control systems. You will serve as a technical lead within the team for any process control issues generated by Programmable Logic Control (PLC), Environmental Monitoring systems … participate in safety reviews, Failure Modes and Effects Analysis (FMEAs), HAZOPS, or similar Maintain records for regulatory purposes to current legislation, including Current Good Manufacturing Practice (cGMP) where required Support vendor cost negotiations/challenge cost increases/scope Ensure the maintenance team are educated on new equipment and involved ...

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 ...

SEKISUI Diagnostics in Maidstone, UK seeks a Senior Controls System Engineer to lead design, delivery, validation and lifecycle management of GMP-compliant control systems. You will guide PLC/SCADA development, FAT/SAT testing and ensure traceability from URS to code while partnering with QA and Operations. The role … requires strong GMP experience, P&ID interpretation and ability to manage multiple projects in a fast-paced environment, delivering compliant automation solutions across site assets. #J-18808-Ljbffr ...

sponsors on some of the most complex data challenges facing UK pension schemes. Working closely with clients, you will lead and deliver projects across GMP Equalisation, benefit rectification, data audits, data remediation, buy-in and buy-out readiness, pensions dashboards and wider de-risking initiatives. In this client-facing role … pensions knowledge with a consultative approach, excellent stakeholder management skills and the ability to build trusted relationships with trustees, sponsors and advisers. Experience of GMP Equalisation, benefit audits, data remediation, buy-in/buy-out activity or wider pensions data consulting projects is essential. Apply here or get in touch ...