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Smart4Sciences are currently working with a global analytical research and testing provider to recruit a Quality Manager GMP their MHRA, FDA AND UKAS regulated facility in Kent.
As a Quality Manager you will be a key part of the site leadership team and responsible for all QA functions including processes, systems and staff - liaising with other Quality Managers across the group to ensure a unified approach to quality across all global sites.
Key responsibilities
- Oversee the site QA function, ensuring compliance with GMP, ISO 17025, FDA 21 CFR 820, and other regulatory standards.
- Lead a team of Quality Specialists, promoting a positive culture of quality compliance and upskilling staff members through regular coaching/training
- Lead investigations, audits, non-conformances, and supplier quality to drive continuous improvement
Key Requirements
- Significant experience in GMP Quality Assurance from the Pharmaceutical and/or Medical Device industries including management and leading of teams
- A demonstrable background in continuous improvement with a proficiency in Six Sigma and Lean Methodologies
- Prior experience in a CRO/CDMO environment with the ability to manage multiple priorities in busy project based environments.
Interviews for this Quality Manager position are imminent so please apply today or contact Gareth Gooley at Smart4Sciences for more information
