- Join an established and growing medical products business operating within the advanced wound care and infection prevention sector.
- Work in a friendly, collaborative office environment where your voice is heard, your ideas are valued and you can work closely with colleagues across the business.
- A hands-on opportunity to make a genuine impact on quality, compliance and continuous improvement within a regulated medical device environment.
About the company
An established medical products manufacturer specialising in advanced wound care and infection prevention, developing products designed to improve patient care and support healthcare professionals. The business has a strong focus on quality, innovation and continuous improvement.
About the role
We are looking for a Quality Engineer with at least 2 years’ experience within medical device or medical product manufacturing. You will support and maintain the effectiveness of the QMS, ensuring compliance with relevant regulations and standards while supporting investigations, audits, CAPA, supplier management, product release and ongoing quality improvements.
The role is based at the company’s head office in Northwest London and requires 5 days per week in the office.
Requirements
- Minimum 2 years’ Quality experience within medical device or medical product manufacturing.
- Practical experience working within an ISO 13485 / medical device QMS.
- Strong knowledge of CAPA, Document Control, Change Control, Risk Management, Internal Audits and Product Release.
- Understanding of applicable medical device regulations and international standards.
- Experience with supplier/subcontractor quality management and reviewing quality documentation.
Package
- £50,000-£55,000 + bonus
- 25 days holiday + bank holidays
- Learning & Development and career progression opportunities
- Employee Assistance Programme and wellbeing support
- Online GP through Livi
- Lifestyle discounts and team-building events
#J-18808-Ljbffr…