7 of 7 GMP Jobs in the Thames Valley

Acting as an internal & external Veeva technical expert with detailed in-depth knowledge of the system configurations and their relationship to ensure compliance with GMP Partnering with OXB Validation department to ensure the Veeva Vault system retains its validated status throughout its lifecycle Owning the solution strategy for the delivery ...

will provide strategic leadership for the IFS product roadmap, ensuring its alignment with organisational objectives, timely and high-quality delivery and adherence to GMP compliance standards where needed, playing a key part in advancing our mission and making a real difference. Please note, this is a hybrid opportunity based ...

quality standards. Ability to embed risk management principles and compliance requirements across teams. Experience within the Pharmaceutical industry or a similar regulated industry (GxP, GMP etc) is highly desirable but not essential. ...

ideal candidate is a seasoned, commercially-minded analytics expert with hands-on experience across the Google Cloud and Google Marketing platforms (BigQuery, Looker, GA4, GMP). They must have a proven track record in client consulting, the ability to advise senior stakeholders and experience of building an analytics practice centered ...

work directly with clients to analyse, cleanse and migrate data, design and test Pension calculations, and support key industry programmes such as GMP rectification and equalisation. Key Responsibilities Analyse complex Pensions data using SQL and Excel Deliver data mapping, migration and cleanse activities Produce and test calculation specifications based ...

Review Deviations, CAPAs, Change Controls and Supplier Complaints Review Computer Systems Validation (CSV) documents Identify and lead QMS improvements Monitor and produce metrics for GMP compliance Deliver training on QMS Profile description: We are looking for: A-Level education in (science preferred) or equivalent experience Experience working within a GMP … Knowledge of pharmaceutical regulations and compliance requirements Experience within Quality within a pharmaceuticals environment Hands-on experience using electronic Quality Management Systems (eQMS) to GMP standards. An understanding and awareness of Computer Systems Validation (CSV) An understanding of Quality audits, investigations, and root cause analysis and change Control Processes Proficient ...

Respectful . Were currently recruiting for a Manufacturing Equipment & Systems Specialist to join our Manufacturing Team . In this role, you willensure compliance of GMP Equipment & Systems within the manufacturing department enabling efficient batch delivery against production schedule in line with GMP, safety and environmental requirements, playing a key part … Systems We are Looking For: A-Level, preferably science based with previous industrial experience Graduate in STEM subject (preferred) Experience working in a GMP environment Experience working with of Cell & Gene therapy manufacturing equipment and systems. e.g. bioreactors, chromatography, clean rooms etc. Ability to travel across all Oxfordshire sites Willingness ...