Quality Management Systems / CAPA Specialist

JR United Kingdom; England; On-site; GBP 35,000 - 50,000; Full time

Job summary

A leading Medical Device Manufacturer seeks a Quality Management Systems Specialist in Gloucestershire. The role involves managing the internal audit program and supporting the ISO 13485 certified Quality Management System. Candidates should have experience in Quality Systems, preferably in the Medical Devices industry, and strong communication skills.

Qualifications

• Experience with Quality Systems is essential.
• Experience in the Medical Devices industry is highly desirable.
• Excellent written and oral communication skills in English.

Responsibilities

• Manage the internal audit program, including scheduling audits.
• Lead and support continuous improvement projects.
• Provide training to team members as required.

Skills

Quality Systems

Communication

Continuous Improvement

Tools

Microsoft Office

Job description

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Quality Management Systems / CAPA Specialist, Gloucestershire

Client: Cpl Life Sciences

Location: Gloucestershire, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Views:

1

Posted:

23.05.2025

Expiry Date:

07.07.2025

Job Description:

Our client, a leading Medical Device Manufacturer, is looking to appoint a Quality Management Systems (QMS) specialist responsible for managing the internal audit program. The role supports the implementation and maintenance of the ISO 13485 certified Quality Management System across the company, including Quality Objectives, NC/CAPA management, and monitoring, measuring, and reporting on QMS performance.

Responsibilities of the Role:

1. Manage the internal audit program, including scheduling audits and assigning auditors.
2. Perform internal audits as assigned.
3. Manage the Quality Objectives procedure.
4. Manage the NC/CAPA procedure.
5. Provide backup/support for document control and training activities on MasterControl.
6. Provide training to team members/colleagues as required.
7. Perform other duties as required.
8. Lead and support continuous improvement projects.
9. Ensure awareness and understanding of health & safety responsibilities as per company policy, and cooperate in statutory compliance.

Qualifications and Experience:

• Experience with Quality Systems is essential.
• Experience in the Medical Devices industry is highly desirable.
• Proficiency in Microsoft Office (Word, Excel, OneDrive).
• Excellent written and oral communication skills in English.