We are seeking a highly experienced and motivated Manager, Regulatory Affairs, to join our growing Regulatory Affairs team. This role is critical to ensuring compliance with U.S. regulatory requirements and supporting the development, approval, and lifecycle management of medical devices. The ideal candidate will possess deep expertise in U.S. FDA regulations, a good general understanding of EU MDR and international standards, and will contribute to strategic regulatory planning and execution.
Responsibilities
- Lead regulatory strategy and submissions for Class II and III medical devices in the U.S.
- Prepare and manage regulatory submissions including 510(k), PMA Supplements, and annual reports.
- Serve as the U.S. regulatory lead on cross-functional project teams, ensuring alignment with clinical, quality, and R&D functions.
- Interpret and apply regulatory requirements to product development, labeling, and review of advertising and promotional materials.
- Monitor changes in regulatory requirements and communicate impact to internal stakeholders.
- Support audits and inspections by regulatory authorities.
- Lead post‑market regulatory assessments and submissions, including periodic reports, vigilance reporting, and regulatory renewals.
- Manage complaint handling activities, ensuring timely investigation, documentation, and regulatory reporting in compliance with applicable standards.
Requirements
- Bachelor’s degree in engineering, life sciences, pharmacy, or a related field. An advanced degree is preferred.
- Minimum 10 years of experience in regulatory affairs within the medical device industry.
- Proven track record of successful submissions to the FDA.
- In‑depth knowledge of FDA 21 CFR 820, ISO 13485, and other applicable standards.
- Strong communication, leadership, and project‑management skills.
- Experience with eQMS systems and electronic document control is preferred.