9 of 9 Permanent GMP Jobs in the East of England

communication, attention to detail and presentation skills Experience creating personas, user journeys, process flows, wireframes, and/or interface mockups Experience in GxP/GMP project process and deployment Experience in handling data migration, system upgrade and cloud hosting project deliveries Data Modelling expertise Product/system/process validation ...

communication, attention to detail and presentation skills Experience creating personas, user journeys, process flows, wireframes, and/or interface mockups Experience in GxP/GMP project process and deployment Experience in handling data migration, system upgrade and cloud hosting project deliveries Data Modelling expertise Product/system/process validation ...

validation activities of the QMS software utilizing a risk-based approach. Ensure compliance to medical device industry regulations, including 21 CFR Part 11, EU GMP Annex 11, and EU GDPR. Supply Chain Responsibilities: • Validate, implement, manage, and maintain an ERP System that is compliant with regulatory requirements in applicable regions ...

validation activities of the QMS software utilizing a risk-based approach. Ensure compliance to medical device industry regulations, including 21 CFR Part 11, EU GMP Annex 11, and EU GDPR. Supply Chain Responsibilities: • Validate, implement, manage, and maintain an ERP System that is compliant with regulatory requirements in applicable regions ...

validation activities of the QMS software utilizing a risk-based approach. Ensure compliance to medical device industry regulations, including 21 CFR Part 11, EU GMP Annex 11, and EU GDPR. Supply Chain Responsibilities: • Validate, implement, manage, and maintain an ERP System that is compliant with regulatory requirements in applicable regions ...

validation activities of the QMS software utilizing a risk-based approach. Ensure compliance to medical device industry regulations, including 21 CFR Part 11, EU GMP Annex 11, and EU GDPR. Supply Chain Responsibilities: • Validate, implement, manage, and maintain an ERP System that is compliant with regulatory requirements in applicable regions ...

related to CSV to improve inhouse CSV process by identifying areas for enhancement and implementing best practices. Must possess understanding of GCP, GLP, and GMP principles and procedures. Must possess excellent verbal and written communication skills. Proficient in MS Word and other Office applications. A strong team player with ...

biology, biomedical sciences) or equivalent. Proven experience in quality assurance within a regulated manufacturing or laboratory environment. Strong knowledge of quality systems, ISO standards, GMP/GDP principles, and regulatory compliance. Skilled in leading audits, managing CAPAs, and interpreting quality metrics. Excellent leadership, communication, and problem-solving abilities. Proficient ...

Senior Lab Systems Lead, supporting Lab Execution System (LES) deployment. We are seeking highly motivated and organised individuals with previous experience of instrumental methods, GMP testing activities, and data management systems such as Chromatography Data Systems (CDS) or Laboratory Information Management Systems (LIMS). This role is suited to hybrid … Serve as the interface between lab users and IT for system deployments (e.g., LES, LIMS, CDS) Optimize laboratory application usage and ensure compliance with GMP standards Support digital transformation initiatives within regulated environments What We’re Looking For Degree in a relevant scientific discipline, for example, Chemistry, Pharmaceutical or Biological ...