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We are seeking a motivated individual to join a well-established company in the South of England. This role involves managing a small technical team with responsibilities covering Product Release, Quality Investigations, Auditing, Change Control, Customer Complaints, CAPA, and Raw Materials and Component Release. You will also lead the supervision, training, and performance appraisal of QA personnel.
Key Responsibilities:
- Oversee QA workload planning to align with business requirements, including all validation, calibration, and maintenance activities within the facility.
- Enhance Quality Systems to improve the speed and efficiency of delivering technical information.
- Manage both internal and external audit systems to ensure compliance and timely audit completion.
- Coordinate risk assessments, implement change controls, and drive continuous improvement initiatives.
- Support process capability studies and apply statistical techniques as needed.
- Ensure full implementation of company policies, including HACCP plans, Quality Plans, Supplier and Raw Material Approval, Equipment Calibration, Customer Complaint Management, and more.
Qualifications:
- BSc in Chemistry, Biochemistry, or a related field; a Diploma in Quality is preferred.
- Several years of experience as a QA scientist in pharmaceutical, medical device, or biologics manufacturing.
- Proven experience in a cGMP environment with a strong understanding of document control systems, auditing processes, and familiarity with MHRA and FDA regulations.
The position offers an excellent salary and above all, the ability to work with a highly successful team.
The candidates must have excellent communication skills as they will be expected to liaise with staff at all levels.
To apply for this position, candidates must be living in the UK and eligible to work.
