Quality Improvement Lead – GMP & CAPA Expert

CooperVision; Eastleigh; Presencial; GBP 42 000 - 54 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

25 days holiday

Pension scheme

Healthcare cover

Life assurance

Wellness Platform access

Discounted contact lens scheme

Resumo da oferta

CooperVision is seeking a Quality Improver to lead investigations, drive continuous quality improvement, and ensure compliance across Packaging & Distribution. You will collaborate cross-functionally to implement corrective and preventive actions and support GMP initiatives.

The role is based in Mountpark, Eastleigh, with a full-time schedule Monday to Friday. Candidates should have experience in regulated environments and knowledge of ISO14971 and ISO13485.

Qualificações

• Minimum of 1 year experience in a regulated industry.
• Experience in Quality or Engineering is an advantage.
• Knowledge of Contact Lens and Packaging & Distribution processes.
• Knowledge of ISO14971 and risk management to medical devices is beneficial.

Responsabilidades

• Represent QA in NCR, Quality Feedback, Customer Complaint and SNC investigations.
• Lead quality improvement projects and drive continuous improvement initiatives.
• Lead CAPA teams to ensure timely investigations and effective corrective actions.
• Provide GMP training and support GMP improvement projects.
• Develop and maintain documentation and procedures.

Conhecimentos

Quality improvement

ISO 14971

ISO 13485

Regulated industry experience

Communication skills

Driving licence

Ferramentas

GPS

Baan

Red Prairie

Agile

Microsoft Office

Descrição da oferta de emprego

CooperVision is seeking a Quality Improver to lead investigations, drive continuous quality improvement, and ensure compliance across Packaging & Distribution. You will collaborate cross-functionally to implement corrective and preventive actions and support GMP initiatives.

The role is based in Mountpark, Eastleigh, with a full-time schedule Monday to Friday. Candidates should have experience in regulated environments and knowledge of ISO14971 and ISO13485.