13 of 13 Permanent GMP Jobs in England

compliance with internal and customer standards. Manage traceability, non-conformances, corrective actions and customer complaints, ensuring timely investigation and robust follow-up. Ensure regular GMP, hygiene, fabrication, and internal audits are completed to schedule, with clear communication of findings and close-out of actions. Work collaboratively across departmentsincluding Operations, Engineering ...

including workflows, benefit calculations, member records, letters, and software updates. Assist with data projects and reporting, such as pension dashboard implementation, scheme data extracts, GMP equalization, benefit statements, and pension increases. Contribute to the transition to the new global payroll system, development of interfaces, and ensure accurate member record updates ...

under instruction. Strong proficiency in MS Office (Word/Excel) is critical, along with superb interpersonal skills, both verbal and written. An understanding of GMP work is also crucial for this position. #LI-TM2 Compensation and benefits On top of a competitive salary, great teams and exciting career opportunities ...

under instruction. Strong proficiency in MS Office (Word/Excel) is critical, along with superb interpersonal skills, both verbal and written. An understanding of GMP work is also crucial for this position. #LI-TM2 Compensation and benefits On top of a competitive salary, great teams and exciting career opportunities ...

under instruction. Strong proficiency in MS Office (Word/Excel) is critical, along with superb interpersonal skills, both verbal and written. An understanding of GMP work is also crucial for this position. #LI-TM2 Compensation and benefits On top of a competitive salary, great teams and exciting career opportunities ...

structured problem-solving techniques such as 5 Whys and fishbone diagrams Lead process control and technological excellence - Implement and sustain process standards and GMP requirements, ensuring consistent process control strategies are in place. You'll act as the technical expert for your line, driving improvements in efficiency and product quality ...

understanding of IT Qualification activities would be beneficial. An understanding of Electronic Records and Electronic Signatures, e.g. USA 21 CFR Part 11, EU GMP Guidelines, Chapter 4, Annex 11 and GAMP 5. An understanding and appreciation of a Quality Management role within an IT Organisation, in particular the Software Development ...

Complete all service reports, calibration records, and regulatory documentation accurately and on time. Adhere to all company, customer, and regulatory health & safety requirements, including GMP, GLP, and relevant ISO standards. Other areas of responsibility Expected to support with other tasks where necessary. Package and benefits Salary £35 - £45,000 depending ...

across raw materials, production processes, and finished products. Maintain accurate and compliant documentation in line with industry and company standards. Ensure adherence to HACCP, GMP, and site-specific quality procedures. Support internal and external audits through meticulous record-keeping and process compliance. Investigate non-conformances and assist in implementing corrective ...

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: Nights: Monday ...

Services, Senior Pharmacists, technical leads and other external service providers/contractors, to develop and maintain the aseptic service provision, and Good Manufacturing Practice (GMP) regulatory requirements for unlicensed activity. Responsible for the provision of technical support and advice on medicines quality/quality assurance matters to all areas … with clear career pathways and access to further education. Key Duties Quality Assurance To lead and maintain systems based on quality assurance requirements for GMP activities under the Medicines Act 1968 Section 10 exemption for unlicensed activity and for GDP activities under the MHRA WDA(H) licence. Ensure efficient ...

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 ...

both technical and stakeholder-facing teams. You will play a key role in delivering high-profile transformation projects such as data cleanses, benefit rectification, GMP reconciliation/equalisation, and system implementations. Key Responsibilities: Lead the technical delivery of complex pension data and calculation projects. Define technical approaches and delivery strategies … individual member calculations. Proven experience delivering bulk pension data and/or calculation projects. Experience leading or heavily influencing pensions transformation projects (e.g. GMP reconciliation, GMP equalisation, benefit rectification, risk settlement data cleanse, system implementation). Advanced Excel skills, including building and reviewing calculation models. Strong problem-solving and analytical ...