9 of 9 GMP Jobs in the South East

validation computer systems - very desirable. Quality experience in a pharmaceutical environment A degree (or equivalent) in a scientific discipline (desirable). Clear understanding of GMP or any other GxP area, regulatory and accreditation systems, and quality management. Excellent analytical thinking to evaluate information and understand complicated issues. Excellent interpersonal skills ...

product assessments Support product launches, data tracking and continuous improvement initiatives Maintain responsibility for site pest control and audit readiness Ensure completion of hygiene, GMP, fabrication and calibration audits through the QA team Manage microbiological sampling, swabbing and testing programmes Conduct traceability exercises and support complaint investigations Drive improvements ...

with required standards. Responsibilities include monitoring and enforcing quality control measures, conducting quality audits, managing quality systems, and ensuring adherence to Good Manufacturing Practices (GMP). You will collaborate with cross-functional teams to promote a culture of quality excellence across all operations. Qualifications Experience with Quality Management and Quality ...

embedding Greencore, customer, and legal standards, ensuring compliance is consistently achieved and maintained. This role plays a critical part in driving improvements in GMP performance and audit readiness, helping to raise quality standards and strengthen food safety culture across the site. Role Accountabilities Understand and apply Greencore, customer ...

critical cooling infrastructure Familiarity with BMS platforms (e.g. Trend, Tridium Niagara) IOSH qualification or equivalent Experience working in audit-driven environments (GLP/GMP) Additional experience that would be beneficial includes working within laboratory and cleanroom environments while following gowning and contamination control procedures, participating in on-call support ...

resolving any inconsistencies or errors Supporting the development and maintenance of internal spreadsheets Assisting with large-scale projects, including pension-related initiatives such as GMP equalisation Performing basic calculations to validate system outputs Providing support with system maintenance tasks (e.g. password resets, report generation) Participating in team meetings, training sessions ...

business. The successful candidate will play a key role in maintaining and continuously improving the Quality Management System (QMS), ensuring compliance with GDP/GMP requirements, and supporting regulatory obligations in line with MHRA, Home Office, and EU regulations. This role requires a strong understanding of pharmaceutical quality systems, supplier … maintaining GDP compliance and WDA obligations Ensure continuous monitoring and improvement of the Quality Management System (QMS) Ensure compliance with MHRA, Home Office, GDP, GMP, and EU regulatory requirements Provide QA support across all departments to ensure regulatory compliance is maintained Support recall management, incident handling, and escalation processes Quality ...

improvement initiatives focused on process simplification, standardisation, efficiency, and scalability Ensure harmonised QMS processes comply with applicable regulations and standards including FDA, ISO 13485, GMP, GDP, and regional regulatory requirements Technical Responsibilities: Apply structured PMO and project management methodologies across enterprise quality transformation initiatives Track completion of harmonisation milestones, remediation … Experience supporting regulatory inspections, remediation programmes, audit readiness, and compliance transformation activities Strong understanding of global quality regulations and standards including FDA, ISO 13485, GMP, GDP, and related quality system requirements Experience with enterprise quality systems, digital quality platforms, and governance frameworks preferred Experience with Lean, Six Sigma, or continuous ...

supplier approval, including SAQs, audits, and certification requirements • Support and lead raw material elements of internal, customer, and group audits • Audit compliance with QMS, GMP, and HACCP standards, driving corrective actions to closure • Monitor KPIs, identify trends, and drive continuous improvement initiatives • Communicate customer and business requirements clearly to suppliers … ensure compliance and robustness • Ability to work cross-functionally with Technical, Operations, NPD, and suppliers • Strong audit capability with a clear understanding of GMP and HACCP requirements • Highly organised with excellent attention to detail • Strong communication skills, able to influence at all levels • Proactive mindset with the ability to anticipate ...