Job Description
The Position
The Principal Scientist (Director), CMC Regulatory Affairs – Medical Devices & Combination Products provides strategic leadership and execution for global regulatory activities supporting medical devices, drug-device combination products, and associated CMC regulatory programs across development, registration, commercialization, and lifecycle management. This role serves as the senior regulatory lead for complex device and combination product programs, shaping global regulatory strategy, influencing development and manufacturing decisions, and ensuring successful regulatory outcomes that support business objectives, patient access, and uninterrupted product supply. The Director reports to the Executive Director, and partners closely with Product Development, Device Engineering, Pharmaceutical Development, Quality, Manufacturing, Supply Chain, Clinical, Safety, Commercial, and Global Regulatory Affairs organizations to navigate complex and evolving regulatory requirements while advancing innovative products through the global regulatory landscape.
This position requires a strategic thinker who can influence senior stakeholders, resolve complex regulatory challenges, and lead regulatory approaches where precedent may be limited or regulatory expectations are evolving.
Responsibilities
Regulatory Strategy Leadership
Develop and lead global CMC regulatory strategies for medical devices and drug-device combination products across all stages of the product lifecycle.
Drive regulatory approaches supporting development, clinical investigation, registration, commercialization, lifecycle management, and patient supply continuity.
Provide strategic regulatory guidance for complex device technologies, delivery systems, connected devices, and combination products.
Anticipate regulatory risks and develop mitigation strategies to support program objectives and business priorities.
Lead resolution of complex regulatory issues where regulations are evolving or established regulatory precedent is limited.
Global Regulatory Execution
Lead regulatory strategy and execution for major submissions and regulatory milestones, including: INDs and CTAs
NDAs, BLAs, and MAAs
Device constituent documentation
Notified Body submissions and opinions
Significant post-approval changes
Global lifecycle management submissions
Oversee regulatory impact assessments for manufacturing, design, process, packaging, labeling, and device constituent changes.
Ensure regulatory requirements are integrated into development plans, control strategies, and commercialization activities.
Medical Device & Combination Product Leadership
Serve as the primary regulatory expert for medical device and combination product requirements.
Provide strategic oversight for: Design controls
Risk management
Human factors engineering
Usability validation
Clinical and performance evaluations
Device verification and validation activities
Labeling and Instructions for Use (IFU)
Post-market regulatory activities
Guide teams on global requirements applicable to Class II and Class III devices, disposable medical devices, and combination products.
Ensure alignment of device constituent strategies with drug and biologic regulatory pathways.
Health Authority Engagemen t
Represent Regulatory Affairs during interactions with FDA, EMA, Health Canada, Notified Bodies, and other global regulatory agencies.
Lead strategy development, briefing preparation, agency responses, and regulatory negotiations.
Provide leadership during inspections, audits, and regulatory inquiries involving device and combination product requirements.
Influence regulatory approaches through effective engagement with health authorities and industry stakeholders.
Cross-Functional Leadership
Act as a strategic partner across Product Development, Manufacturing, Quality, Clinical, Safety, Supply Chain, Commercial, and Regulatory organizations.
Influence key development and lifecycle decisions through expert…