8 of 8 GAMP Jobs in the UK excluding London

environment and/or software development environment. Experience integrating instruments via serial/USB/Ethernet connections. Knowledge of Oracle databases. Understanding of GMP, GAMP or regulated software validation. Experience delivering customer training. Full UK driving licence. What we offer Career development and professional growth opportunities. Competitive salary. You will ...

downtime events, and process deviations. Cybersecurity & Compliance — Ensure systems meet site standards for safety, cybersecurity, and regulatory compliance (e.g., IEC 61131‐3, ISA‐95, GAMP). Continuous Improvement — Identify automation opportunities to improve throughput, quality, and reliability. Cross‐functional Collaboration — Work with production, maintenance, quality, and IT teams to deliver ...

critical healthcare systems used globally. Keywords: Radiopharmacy, Nuclear medicine, PET/SPECT, LIMS, Project delivery, System implementation, Validation (IQ/OQ/PQ), GMP, GAMP 5, 21 CFR Part 11, Annex 11, Compliance, SME, Customer-facing, Stakeholder management, Training, UAT, Software validation, IT systems, Deployment, Upgrades, Support, Process improvement ...

project plans with key milestones. Ensure that all machinery supplied or modified is safe and in accordance with EC and UK regulations, harmonised standards, GAMP guidance and client standards. Develop the software and control systems for machines during commissioning in a structured and controlled way. Ensure all software and design ...

project plans with key milestones. Ensure that all machinery supplied or modified is safe and in accordance with EC and UK regulations, harmonised standards, GAMP guidance and client standards. Develop the software and control systems for machines during commissioning in a structured and controlled way. Ensure all software and design ...

world leader in the design, engineering and installation of pharmaceutical-grade systems. Duties Design and development of control systems. This will include working to GAMP 5 requirements including the preparation/reviewing of URS, FDS, SDS, HDS, FAT and SAT documents. Design and development of Software code primarily for Siemens ...

overall compliance oversight for all GxP computerised systems across Pharmanovia Ensure systems comply with regulatory expectations, including EU Annex 11, 21 CFR Part 11, GAMP and MHRA data integrity guidance Develop, implement and maintain computerised systems validation and lifecycle management processes Act as the organisation’s subject matter expert … Deviation, Change Controls, Complaints, PQRs, Management Reviews, recalls, Strong knowledge of: Good Manufacturing Practice (GMP) and GxP EU Annex 11 21 CFR Part 11 GAMP 5 Data integrity principles and MHRA expectations Experience supporting or leading regulatory inspections and audits Required Skills Ability to translate complex technical and regulatory concepts ...

process manufacturing environment, with exposure to: PLC/SCADA/DCS systems (Rockwell/DeltaV environments) Batch control systems and automation strategies GMP/GAMP/21 CFR Part 11 compliance Process equipment such as: filtration systems fluid handling systems bioprocess-style equipment Clean utilities and building systems (HVAC, purified … complex process control systems Desirable Experience Exposure to platforms such as DeltaV, FactoryTalk or ControlLogix Experience with batch processing and process automation Knowledge of GAMP, 21 CFR Part 11, S88/S95 Experience with: bioprocessing systems CIP/COP/autoclaves cleanroom or controlled environments Why This Role? Be part ...