8 of 8 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 ...

Analytics or QA Operations team within QA. The purpose of the role is to provide QA support for either the Oxford Biomedica's GMP Laboratory testing facilities or GMP Manufacturing facilities. Oxford Biomedicas Quality Assurance (QA) team is responsible for the companys quality processes and systems, in compliance with GMP … internal and external audits, quality compliance and control. This is a 9IC grade Your responsibilities in this role would be: Oversee quality of GMP testing operations or GMP manufacturing operations to ensure adequate and timely release of GMP compliant product. Ensures that all documentation and quality records are reviewed ...

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 ...

product direction across cross-functional, multi-region teams. A strategic thinker capable of shaping long-term transformation while executing fast. Comfortable in complex, regulated, GMP-heavy environments. Experience delivering solutions that optimise: Manufacturing performance Supply chain planning Network strategy Quality workflows Data governance & AI compliance Why This Role Matters This ...

solving tools such as Fishbone, 5 Whys etc. Authors, reviews, and approves Controlled Documents in accordance with procedures. Will support in delivering the site GMP training as required. Will conduct the internal audit programme. Will support the maintenance of the site QMS and facilitate reporting of relevant KPIs within department … investigated and communicated. The Person:- The ideal Candidate will hold a degree in a STEM related subject Experienced in batch review and batch release GMP QA experience is essential! Ideally in a Pharmaceutical setting or similar Experience in CAPA, deviations, change controls, internal auditing (preferred) etc Strong interpersonal skills ...

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. ...

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 ...