12 of 12 CAPA Jobs in the UK

development (Phase I/II) projects Experienced in batch record review processes including the review and approval of batch documentation and associated documentation. Experienced in change control, deviation and CAPA management. Experienced in reviewing calibration and qualification documentation. Experienced in working with cross functional teams to identify and implement changes and improvements within pharmaceutical manufacturing and warehousing environments. Must have More ❯

Officers to ensure product release meets GMP and QMS standards. Support the QA Manager with site inspections, internal audits, and external regulatory visits. Oversee documentation control, SOP reviews, and CAPA implementation. Drive continuous improvement initiatives and training programmes across the QA team. Deputise for the QA Manager when required, maintaining high standards of compliance and communication. Collaborate with cross-functional More ❯

performance and performance trends assessed to understand and drive improvement opportunities. QMS Administration - Sr. Quality Assurance Engineers are responsible for conducting QMS administration activities, including Internal Quality Audits, Corrective and Preventive Action, Process Change Control, Exception Handling, process improvement and maintenance, supplier quality, external audit support, and related activities. The Sr. Quality Assurance Engineer shall follow the guidance of RA More ❯

manufacturing or production environment - precision environment Strong knowledge of quality standards and regulations such as ISO, GMP, FDA if applicable). Experience with quality tools and methodologies such as CAPA, FMEA, Root Cause Analysis Certification in quality management systems - desirable Excellent communication, analytical, and problem-solving skills. Ability to manage multiple priorities and work effectively across departments Apply: To apply More ❯

standards (ISO9001 essential) Proven track record in supporting audit close-outs and corrective actions Experienced in documentation, process improvement, and stakeholder engagement Skilled in Root Cause Analysis tools and CAPA management Assertive communicator with the ability to influence and support stakeholders across all levels Agile, flexible, and proactive approach to problem-solving Degree in Engineering, Quality or related field - open More ❯

meetings and the management of the meetings outputs. Supporting Regulatory, ISO and Client audits, and conducting Supplier audits, internal audits, and self inspections, including the preparation of responses and CAPA plans. Key Skills/Experience/Requirements: Strong organisational and communication skills, with excellent attention to detail. Ability to show initiative and be proactive, working well under pressure and to More ❯

Collaborating across internal departments to provide Quality Assurance support. Participating in external Quality aud it activities . R epresenting QA for various projects across the Basingstoke sites. Supporting with CAPA, Complaints, R&D QA, I nternal audits , change management , De viations Supporting R&D for new product introductions. Reporting on the performance of the Quality system for the site What More ❯

documentation, auditing, or compliance desirable. GCSEs (or equivalent) in English and Maths; further education or quality-related training advantageous. Keywords: Quality Assurance, QA Assistant, Manufacturing, ISO 9100, Document Control, CAPA, NCR Please contact Ryan Taylor on 0161 746 3311 at Winsearch for more information. Winsearch acts as an employment agency for permanent staff. We recruit for roles in Engineering and More ❯

Cargo Inspection Systems and its Sub Systems. Establish and sustain a thorough and workable Service Routines, Troubleshooting and Fault-finding Guides for the Mobile Systems. Provide the Mobile Systems CAPA and ECN interface between Cargo Service and Cargo Engineering. Advise on suitable, scalable, and achievable Mobile System Spares Packages covering Service Consumables, Critical Parts, and Stock guides. Provide support to More ❯

and support crisis response initiatives. Ensure compliance with quality management systems (QMS), GxP, and financial policies. Oversee customs data, export control activities, and monitor regulatory changes. Support audits, maintain CAPA and regulatory trackers, and ensure global compliance. Contribute to continuous improvement initiatives and represent logistics in cross-functional projects. Track and improve service provider KPIs, optimise lead times, and resolve More ❯

tasks related to pharmaceutical products. Ensuring products are fit for purpose before release for use or commercial sale. Maintaining and improving QMS' performance by ensuring items such as deviations, CAPA and change control for which you are the owner are progressed in a compliant and timely manner and all other items are reviewed and/or approved in accordance with … 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, we are looking for Candidates who are good communicators Strong written and verbal use of English language essential due to More ❯

and up-to-date quality and compliance documentation, including SOPs, traceability records, and audit logs. Generate and analyse data/KPIs for management review and continuous improvement. Non-Conformances & CAPA: Investigate and document product non-conformances and deviations. Coordinate the implementation of corrective and preventive actions (CAPA) and manage the "hold" procedure for any non-conforming stock. Training & Mentorship: Assist More ❯