Regulatory Affairs & Quality Systems Lead, Digital Health

A dynamic health-tech firm is seeking a Quality Systems & Regulatory Affairs Specialist to join their team. This role involves preparing and submitting regulatory filings while ensuring compliance with international quality standards. The ideal candidate will have at least 4 years of experience in the medical device industry, particularly with regulatory submissions in key international markets. Strong communication and problem-solving skills are essential for this position, which is based in Boston, MA. A commitment to quality and impactful product delivery is highly valued. #J-18808-Ljbffr