7 of 7 GAMP Jobs in the UK

of automation systems. Understanding of device networking and communication protocols. Experience in installing and servicing large integrated systems. Experience in automation controllers and process control (PLCs, Microcontrollers, knowledge of GAMP 5 is a plus). Software and Protocols : Experience writing protocols in Evoware and Venus software Experience in the design, programming, start-up, commissioning, and troubleshooting of integrated laboratory equipment More ❯

as PMX, PharmaSuite (Rockwell), Syncade-DeltaV MES (Emerson), Werum PAS-X, or similar is strongly preferred. Additional Preferences Understanding of GMP regulations and Computer System Validation (CSV) principles (e.g., GAMP 5, 21 CFR Part 11, Annex 11). Experience authoring and validating Master Batch Records (MBRs) in a regulated environment. Strong documentation skills and attention to detail, with experience in More ❯

In-depth knowledge of systems such as DeltaV DCS, SAP, BMS, PCS, PLCs (Siemens), OSI Pi Historian, and GMP environments. - Understanding of regulatory requirements (e.g. CFR 21 Part 11, GAMP 5). - Strong leadership, collaboration, and stakeholder engagement skills. - Experience in aseptic manufacturing environments (highly desirable). - Fluency in English. Why apply? - Work on a high-visibility project in a More ❯

In-depth knowledge of systems such as DeltaV DCS, SAP, BMS, PCS, PLCs (Siemens), OSI Pi Historian, and GMP environments. - Understanding of regulatory requirements (e.g. CFR 21 Part 11, GAMP 5). - Strong leadership, collaboration, and stakeholder engagement skills. - Experience in aseptic manufacturing environments (highly desirable). - Fluency in English. Why apply? - Work on a high-visibility project in a More ❯

Test Strategies and related artefacts such as Policies and Procedures and managing test activities Knowledge and understanding of the software Lifecycle. Application of the V model as exemplified in GAMP 5 Experience of developing and using automated tools for configuration management and software testing, ideally some experience of SharePoint technologies and data manipulation (preferably JSON and XML) Experience of the More ❯

Specialist will support the Quality Assurance department in maintaining compliance of computerised systems and electronic Quality Management Systems (eQMS). This includes contributing to validation activities in alignment with GAMP 5, Annex 11, and other relevant regulations. The role requires an understanding of Computer System Validation (CSV) principles and practical involvement in regulated environments. Essential Functions To maintain and improve … requirements : None Education and Experience Bachelor's or Masters' degree in Life Sciences, Engineering, Computer Science, or related discipline desirable but not essential. Training in Computer System Validation or GAMP 5 preferred. Computer System Validation training desirable. Knowledge, Skills, and Abilities Proven experience working with ETQ, MasterControl, or similar eQMS platforms - configuration, administration, and user training. Strong working knowledge with … user access, and data integrity in Empower Demonstrable success in leading system migrations or large-scale QMS digitalisation projects. Experience in writing and maintaining validation documentation in line with GAMP 5. Good working knowledge of Computer System Validation. Familiar with electronic quality management systems (eQMS). Familiar with environmental monitoring systems. Experience working within a Quality function on computer systems More ❯

on DCS/PLC systems within a pharmaceutical manufacturing site. Develop and implement validation documentation including URS, IQ, OQ, PQ, and validation plans. Ensure compliance with regulatory requirements (e.g. GAMP 5, FDA 21 CFR Part 11, EU GMP Annex 11). Perform risk assessments, impact assessments, and deviation investigations. Collaborate with cross-functional teams including automation, quality, and IT departments. … Validation within the pharmaceutical or life sciences sector. Hands-on experience validating DeltaV systems preferred; other DCS or PLC systems will also be considered. In-depth knowledge of GMP, GAMP 5, and regulatory expectations. Proven ability to author, review, and execute validation protocols and reports. Strong problem-solving, documentation, and communication skills. Ability to work independently on-site in a More ❯