10 of 10 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 ...

continuous improvement across the site. What you will be doing: Lead, coach and develop the site Quality team Ensure full compliance to the FSQMS, GMP, CCPs and process controls Assure all finished products are safe, legal and produced to specification Manage customer complaints, concessions, incidents and escalations Oversee raw material ...

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 ...

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 ...

Automation & CSV Engineer (Permanent) - West Yorkshire Pharmaceutical Manufacturing High-Tech GMP Environment Career Growth Opportunity An exciting opportunity is available for an Automation & Computer System Validation (CSV) Engineer to join a highly regulated manufacturing environment within the pharmaceutical/life sciences sector. This role is ideal for an engineer … maintain automation and control systems across manufacturing operations Troubleshoot equipment and process-related automation issues Participate in computerized system validation (CSV) activities within a GMP-regulated environment Assist with qualification, commissioning, and lifecycle management of automated systems Support continuous improvement and process optimization projects Collaborate with engineering, production, quality ...

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 ...

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 ...

regulated pharmaceutical setting. The role will focus on Emerson DeltaV systems, supporting configuration, integration, and lifecycle delivery of control systems, while ensuring compliance with GMP and data integrity standards. You will work closely with multidisciplinary teams to develop and review key automation documentation, support testing activities, and contribute to system … mechanical, and electrical teams to ensure seamless system delivery Assisting with FAT activities and coordinating with vendors and project stakeholders Ensuring automation activities meet GMP expectations and data integrity standards (e.g. ALCOA+) Taking part in design reviews, HAZOP studies, and risk assessment workshops Managing updates to design documentation through change ...