9 of 9 GMP Jobs in the North of England

Profile Essential ~5 years’ experience in pharmaceutical or medical device manufacturing Background in production, process engineering, or quality Strong understanding of manufacturing operations in GMP environments across multiple products and processes. Excellent communication and problem-solving skills Desirable Exposure to MES or manufacturing digitalisation initiatives Quality Assurance, process improvement ...

activities (IQ/OQ/PQ) for equipment and processes Ensure timely delivery of KPIs and departmental objectives The Person Proven experience within a GMP-regulated environment in a similar QA/Validation role Experience in equipment validations (writing reports), the ideal applicant will have process validation experience too Previous ...

laboratory 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. ...

teams to clearly communicate the requirements for the Store and capture client requirements. The industries we serve have growing requirements for regulatory quality control (GMP, Medical Devices, ISO etc). The System Engineering role provides opportunity to develop the fully documented lifecycle to support adherence to these standards. What ...

completed Collecting micro samples as per schedule Traceability Investigations into complaints Daily auditing of CCPs Daily label checks Calibration Auditing of processing records GMP/Fabric audits Temperature checks Quality checks The nature of the role requires a flexible approach to working hours. Core working hours are: Monday to Friday ...

experience alongside industry‐recognised qualifications. Role To maintain consistent and documented compliance with all relevant Safety, Health and Environmental (SHE), Good Manufacturing Practice (GMP), Data Integrity (DI), quality and best practice requirements To plan and prioritise tasks, review and evaluate progress against objectives and investigate alternative scenarios To identify ...

/AI, and model lifecycle governance; champion reusable data products and platform services. Embed security and compliance: Partner with CISO and QA to integrate GMP/GAMP 5/ALCOA+/GDPR/responsible AI controls; ensure audit‐ready documentation. Provide architectural authority for strategic programs: Shape solution options, simplify … managers and senior architects; set objectives and manage performance. Preferred qualifications Master’s degree and/or TOGAF certification. Background in regulated (GxP/GMP) environments strongly preferred. Experience in biopharma, manufacturing, automation, quality systems, or supply chain is an advantage. 6–10 years’ experience in pharmaceutical/biological manufacturing ...

impact digital transformation projects in the Pharmaceutical industry? This opportunity offers the chance to work on cutting-edge MES implementations and validation strategies within GMP-regulated environments in the UK. Due to upcoming project needs, we are looking for a Senior Consultant – MES & Validation (Siemens Opcenter Execution Pharma … Opcenter Execution Pharma Contribute to the definition of Validation Master Plans and overall validation strategy Review and assess validation documentation to ensure compliance with GMP requirements and project standards Evaluate the system integrator’s project methodology and assess the quality and consistency of deliverables Ensure alignment with project expectations, regulatory ...

product investigations Coordinate and resolve immediate/urgent customer complaints, ensuring prompt responses/resolution Participate in the internal audit programme to ensure continued GMP compliance of all site activities Utilise scientific resources in order to work on improving quality of products and services To maintain personal training folder … Controls CAPAs Deviations Complaints Recalls OOS/OOT The Person: Will have a Degree in a relevant- Scientific discipline Will have good knowledge of GMP Experience in CAPA, Deviations, OOS, OOT, Internal auditing (preferred), Customer Complaints handling would be very advantageous Strong IT skills (Microsoft applications) Good interpersonal skills ...