
Senior QA Officer / Pharmaceuticals / cGMP / Suffolk / £28 - £38k + excellent benefits
Our client is a leading pharmaceutical company based in Suffolk. They are looking to recruit a Senior QA Officer to be responsible for reviewing documentation, maintaining and managing quality systems in line with cGMP and supporting and performing audits and inspections.
Key Responsibilities:
- Reviewing cGMP or regulatory documentation to ensure compliance
- Liaise with internal and external third parties
- Monitor third party compliance
- Provide advice and support to managers and resolve compliance or regulatory issues
- Sign off some cGMP / regulatory documents
- Act as a departmental representative
- Manage quality systems
- Support the continuous improvement process
- Keep up to date with cGMP changes and legislation
- Facilitate internal audits and inspections and produce reports and action plans
- Provide supervision and guidance to less experienced staff
Knowledge Skills and Experience Required:
- Typically a graduate or equivalent and may be working towards externally accredited qualifications
- Ability to successfully facility quality project work or audits
- Demonstrated knowledge / experience of working within a quality management system and cGMP
Salary in line with experience - £27500 - £38k plus excellent benefits.
