6 of 6 GMP Jobs in the South East

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. Your responsibilities in this role would be: Being ...

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 ...

Managers, Responsible Persons and Qualified Persons with the implementation and maintenance of the Quality Management System in accordance with the GMP and GDP guidelines and GPhC, ISO 9001 and ISO 13485 standards. Supporting the ongoing compliance with relevant standards, legal requirements, regulations and the PSDL documented policies and procedures. Promoting … able to promote a positive Quality culture within the company. Excellent knowledge of Word, Outlook, Excel, PowerPoint, and Teams. Good knowledge of GDP, GMP and GPhC regulations, ISO 9001 and ISO 13485 standards. ...

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 ...

understanding and competency. The individual is a training professional whose focus is to train and upskill the production teams and wider business within a GMP environment. The role is responsible for the operational technical training, whilst also supporting EHS and GMP training for the production operation. What are we looking … learning tools to support the delivery of training materials using multiple media types. Knowledge and experience of pharmaceutical packaging and manufacturing operations, including GMP knowledge. Good Communication skills across different levels in the organisation (e.g. Ops, OLT). Strong facilitation, coaching and presentation skills. Training qualification (CIPD, City of Guilds ...