13 GMP Jobs in the South East

this role you must have the right to work in this location. Key Responsibilities: For this role, you will assist with compliance on all GMP/GDP and GCP regulations guaranteeing adherence to GxP and data integrity legislation. Serve as the System Owner/Administrator role for GxP IT systems more »

and contribute to maintaining and developing QMS related to IT. Key Responsibilities: Ensure ongoing compliance of GxP IT systems and processes. Support adherence to GMP/GDP and GCP regulations, including data integrity legislation. Act as System Owner/Administrator for GxP IT systems within QA. Lead Computer System Validation more »

well established Quality team, focusing on the supply chain. We are seeking a detail-oriented and experienced QA officer with a background in pharmaceuticals (GMP) and an understanding of Good Distribution Practice (GDP). The ideal candidate will ensure compliance with regulatory standards, optimize supply chain processes, and uphold company more »

System by supporting global metrics generation and ‘lessons learned from audit/inspection’ · Cover GxP related Functional Areas, specifically thus related to GCP, GVP, GMP and CSV. · Collaborate with the respective Functional Area Heads/representatives · Collaborate with the respective Global and Regional Quality Leads and functions · Ensure the establishment more »

activities. What you'll need to succeed Our client is looking for an individual with strong experience as a Quality Assurance Officer within a GMP Pharmaceutical/Cleanroom environment. Other key desirables include: Quality Management System activities and maintenance. Experience in participating in internal/external audits. Be able to more »

policies. To be proactive in identifying and eliminating faulty processes by implementing long-term fixes. To uphold and exceed standards of product quality and GMP within their area that are appropriate to an industry-leading quality food manufacturer. To play an active role in the shift and be the go more »

developing products used in hazardous environments (i.e. ATEX, nuclear or chemical industries) is preferred but not essential, as would experience of Good Manufacturing Practices (GMP) for the pharmaceutical industry, although neither are essential. Hybrid and flexible working can be discussed. More information available upon application. When applying for this role more »

who is adaptable, can show initiative and pick up lots of new skills quickly Good general laboratory experience, ideally with GLP and/or GMP certification For the chance to join an exciting company on their journey to change the world for the better, please apply today! Bond Williams Professional more »

and on occasions as required If you would like to discuss this further, please contact Mark Bux-Ryan for further information. QP, qualified, person, GMP, manufacturing, sterile, terminally, sterility, aseptic, quality, assurance, manager, leader, MHRA, audit, release more »

focused Extremely safety conscious Helpful and responsive and committed to delivering the very best Team playing whilst proactive and a self-starter Desirable Requirements: GMP manufacturing equipment Recognised formal qualification in secondary control discipline or equivalent experience in Control Systems Knowledge of high integrity PCS and PLC programming would be … Drug Discovery teams. In addition, a Formulation Development team was also recently established. The Hoddesdon site has state-of-the-art Good Manufacturing Practice (GMP) standard facilities for the development of Active Pharmaceutical Ingredients (API), Formulation Development (FD) and Process Chemistry (PC). We offer a competitive salary and a more »

This is a fantastic opportunity to work alongside our industry leading scientists in our GMP accredited laboratories, at our Sandwich facilities (Kent). You will gain a wide range of practical laboratory skills which are supported by our in-house training. Within the Analytical Sciences department in Sandwich, Kent we … of which used to support batch release, and regulatory packages. As such, you will be trained in all these techniques and general AMS and GMP procedures. There will also be a chance to undertake research for Solid Form Screening using some of the abovementioned methodologies. You will be trained to more »

Compliance. Key responsibilities as our Technical & Quality Coordinator: Be a supportive member of the technical department by ensuring compliance with Food Safety, ACCP, Quality, GMP and H&S procedures. Develop and update technical documentation. Conduct internal audits, finished product traces, and support technical team during external audits. Collaborate with cross … Quality Coordinator: Food Technology/Science or equivalent degree Experience in a technical/quality role within food manufacturing Awareness, good understanding of HACCP, GMP, BRCGS standard and food legislation Be highly organised with the ability to work well under pressure and to tight deadlines Have competent IT skills and more »

Summary: The Head of Quality Assurance leads strategic QA efforts, ensuring compliance and driving improvement. They oversee operations, manage teams, and maintain high standards. Responsibilities: Define and drive QA strategy. Set and monitor quality standards. Ensure compliance with regulations. Lead more »