Are you an experienced QA/RA professional ready to lead quality and regulatory strategy in the medical device space?
We're looking for a Quality and Regulatory Manager to oversee our ISO 13485-compliant Quality Management System and ensure global regulatory compliance across UK, EU, US, and Canadian markets. You'll be the designated PRRC under EUMDR 2017/745 and play a key role in driving continuous improvement, managing audits, CAPAs, and post-market surveillance.
✅ What You'll Bring
Degree in Life Sciences or Engineering (BSc/BEng)
Experience in medical device regulatory compliance
Experience with international submissions (UK/EU/US/Canada)
Bonus: Dermatology or microbiology background🌟 Why Apply?
Lead a high-impact team (2 direct reports)
Shape quality culture across the business
Collaborate with global partners and suppliers
Drive innovation in a growing medical device company
Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy