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An exciting opportunity awaits a Quality Systems Engineer at a fast-growing medical device company. This role is pivotal in integrating a newly acquired company's Quality Management System (QMS) into the existing framework. You will focus on maintaining and continuously improving the system, ensuring compliance with global standards such as ISO 13485 and MDR. If you thrive on project ownership and collaboration, this position offers a chance to make a significant impact in a scaling medtech business. Join a dynamic team that values innovation and quality in healthcare technology.
Job Description
I’m working on a fantastic Quality Systems Engineer opportunity with a fast-growing medical device business that’s recently completed an acquisition.
This role will be key in integrating the newly acquired company’s QMS into the existing quality framework. Once integration is complete, the focus will shift to maintaining and continuously improving the system, with a strong emphasis on compliance to global standards like ISO 13485:2016, MDR 2017/745, UK MDR 2002, and 21 CFR 820.
This is a great opportunity for someone who enjoys project ownership, cross-functional collaboration, and making a real impact in a scaling medtech business. If you’d like to hear more or know someone who’d be a good fit, feel free to drop me a message or apply to this advert with your updated CV.