Quality Assurance Manager

JR United Kingdom; Cambridgeshire and Peterborough; On-site; GBP 42,000 - 50,000; Full time

Job summary

An established industry player in the medical device sector is seeking a Quality Assurance Manager to spearhead their quality initiatives. This role involves leading the Quality Department, enhancing the Quality Management System, and ensuring compliance with international regulations. The ideal candidate will have a solid understanding of medical device regulations and proven leadership skills. Join a dynamic team committed to quality and continuous improvement, where your expertise will significantly impact the company's success and growth in the industry.

Qualifications

• Solid understanding of international medical device regulations.
• Proven experience in overseeing quality management systems.

Responsibilities

• Lead the Quality Department, ensuring effective quality assurance.
• Establish and improve the Quality Management System.

Skills

Quality Assurance

Regulatory Compliance

Leadership

Root Cause Analysis

Continuous Improvement

Education

Degree in Life Sciences or related field

Tools

Quality Management System (QMS)

Job description

Social network you want to login/join with:

Quality Assurance Manager, Cambridgeshire

Client:

X4 Life Sciences

Location:

Cambridgeshire, UK

Job Category:

Other

EU work permit required:

Yes

Job Views:

3

Posted:

13.04.2025

Expiry Date:

28.05.2025

Job Description:

Job Title: Quality Manager

Salary: up to £50,000

Job Type: Permanent

A Cambridgeshire based Medical Device company is on the lookout for a Quality Manager to join their growing business. They are looking for an individual that is hard working and self-motivated to assist with all things Quality.

Key Responsibilities:

• Lead the Quality Department, ensuring all quality assurance and control activities are carried out effectively and efficiently.
• Establish, maintain, and continuously improve the Quality Management System (QMS), including conducting audits and supporting regulatory and customer inspections.
• Manage and oversee investigations, root cause analysis, and CAPA processes, driving a culture of continuous improvement.
• Train, mentor, and support QA Technicians and Validation Coordinators, working collaboratively with internal teams to uphold and enhance quality standards.

Experiences and Qualifications Required:

• Solid understanding of international medical device regulations, including CFR 21, EU MDR, UKCA and related market requirements.
• Proven experience in overseeing quality management systems, regulatory compliance, and audit processes.
• Demonstrated leadership capabilities with experience managing teams or leading quality initiatives.

How to apply: Apply to e.smailes@x4lifesciences to learn more about the role or connect with me on LinkedIn to hear about regular job updates available with X4 Life Sciences.