Meet Life Sciences
Quality Assurance Manager
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We are partnering with an established and rapidly growing medical-device manufacturer to recruit an experienced QA Manager.
The company supplies products internationally and has doubled in size over the past six years. Following the acquisition of an additional site, it has ambitious plans for continued growth and expansion into broader medical markets.
This is a business-critical appointment. You will take responsibility for maintaining and developing the Quality Management System while supporting the business through an upcoming MDR submission and future regulatory audits.
The role
You will provide hands-on quality leadership across a growing, multi-site manufacturing business. Alongside managing core quality processes, you will work closely with internal stakeholders and help build a positive, practical quality culture.
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Key responsibilities will include:
- Managing and continually improving the company’s Quality Management System
- Ensuring compliance with ISO 13485 and applicable regulatory requirements
- Leading CAPA, deviation and non-conformance processes
- Overseeing customer complaints and supporting effective investigations
- Supporting MDR submission and audit-readiness activities
- Working collaboratively with manufacturing, engineering and senior stakeholders
- Providing guidance and leadership to members of the quality team
- Ensuring quality processes remain practical and effective within a growing business
- Supporting quality activities across multiple sites
About you
We are looking for someone who combines strong technical quality knowledge with excellent communication and people skills.
You are likely to have:
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- Approximately 5–10 years’ experience in quality assurance
- Experience within medical devices or a closely regulated pharmaceutical environment
- Strong knowledge of ISO 13485 or an equivalent regulated quality framework
- Hands-on experience managing a QMS
- Good knowledge of CAPA, deviations, non-conformances and customer complaints
- Experience communicating with and influencing internal stakeholders
- The ability to lead people and embed a positive quality culture
- A practical, collaborative approach suited to a growing business
- Experience of EU MDR would be advantageous but is not essential.
This is an excellent opportunity to join a successful UK manufacturer at a significant point in its growth and regulatory journey.
Apply now or contact Chris at chris.warman@meetlifesciences.com
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