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