Job Description
The Role
- Support the implementation and maintenance of Quality Systems in line with GMP and corporate standards.
- Review and approve batch documentation, manufacturing records and quality-related documents.
- Manage quality processes including deviations, CAPAs, Change Control and risk assessments.
- Support audits, inspections, validation, product transfers and new product introductions.
- Work closely with manufacturing, QC and other departments to maintain product quality and drive continuous improvement.
- Knowledge of Quality Assurance, Quality Systems and GMP within a pharmaceutical environment.
- Understanding of pharmaceutical manufacturing and packaging processes.
- Experience or exposure to deviations, CAPAs, Change Control or batch documentation.
- Strong communication, problem-solving and organisational skills.
- Confident using Microsoft Office and interpreting technical information.
Our client is a leading global pharmaceutical organisation committed to developing and delivering high-quality medicines.
Apply: If you are interested in this opportunity, please contact Alex Willson ((url removed)), quoting Quality Operations Associate and referencing-71680.
Applicants must have the right to work in the UK.