8 of 8 Permanent GMP Jobs in the North West

related field 3+ years experience in Control Systems Engineering Hands on experience with DCS systems (ideally Siemens SIMATIC PCS7) Previous work experience in a GMP manufacturing environment (Pharmaceutical experience is desireable) Knowledge of GAMP frameworks Willing to work on customer sites across the Northwest Code: INDENM If you are interested ...

within a QA, Quality Assurance, or Quality Control role. Experience within the food manufacturing industry is essential. Good understanding of HACCP, Food Safety, and GMP standards. Strong attention to detail and excellent record-keeping skills. Confident communication skills and ability to work collaboratively. Ability to work independently and make informed ...

experience in programmatic advertising, with a deep knowledge of the Google Stack, Google Ads (Display/Video), DSP (e.g. Adform, Tradedesk, DV360, Amazon DSP), GMP and Analytics Strong understanding of the digital advertising ecosystem, including DSPs, DMPs, and ad exchanges Strong analytical skills and ability to provide insights and recommendations ...

Conveyor Systems and Thermal processing equipment. 3. City & Guilds 2382 (minimum of 18th Edition Regulations) 4. Familiar with the requirements of working within a GMP facility. 5. Excellent internal and external communications skills 6. Experience of working an on-call maintenance system. ...

heights. Making animals’ lives better makes life better – join our team today! Your Role: Advisor, Quality – R&D Position Description: Provides Quality Leadership and GMP compliance guidance across global R&D teams, project groups, and CMOs to support product development, technical transfers, registrations, and successful launches. Partners cross-functionally … Biology, Biotechnology, Chemistry) 5+ years’ experience in Quality Assurance, Quality Control or related technical field (Pharmaceutical Development, Manufacturing, Chemical Engineering etc.) Expert knowledge of GMP and global regulatory requirements (e.g., FDA/CVM, EMA, MHRA/VMD), CMC-related activities, and R&D Quality Assurance from development through registration. Proven ...

Monitoring equipment and facilities to ensure they remain compliant and operational Managing spare parts and consumable stock levels Producing clear, accurate documentation that supports GMP and UKAS requirements Contributing ideas that improve processes, efficiency and reliability This role supports activities across both our Oak Tree House and Coleby House sites … full UK driving licence Bonus Points If You Have Experience With Chromatography systems Mass spectrometry instrumentation Chromatography Data Systems (CDS) Equipment validation and qualification GMP, UKAS or ISO 17025 regulated environments Why Join Us This is an ideal opportunity for someone early in their technical career who enjoys taking things ...

play a key role in data preparation in advance of transactions (e.g. buy‐ins); 2) conduct data audits, benefit audits and calculations; 3) undertake GMP projects. For this reason, prior GMP experience is essential. You will also have a good understanding of the technical aspects of defined benefit pensions, with ...

Elanco is seeking an Advisor, Quality – R&D to provide strategic quality leadership across global R&D teams, ensuring GMP compliance for product development, transfers, registrations, and launches. The role partners across functions to shape quality strategy and optimize systems, training, and processes. The role focuses ...