Hybrid Associate Director, Regulatory Affairs – Medical Devices

Posted 6 days ago

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About the role

  • Develop and communicate RA MD regulatory strategies for projects across the life cycle (Development and On-Market).
  • Ensure device regulatory risks and key issues are communicated in a timely manner to project teams and other stakeholders.
  • Represent department in cross-functional project teams as appropriate.
  • Provide Novartis technical functions clear, concise guidance on current device regulatory requirements to support planning and decision making.
  • Lead and implement global Regulatory Affairs Medical Device (RA MD) submission activities (planning, authoring, reviewing, coordination, submission) for assigned projects/products.
  • Identify the required documentation and content, compliance and timelines issues for global submissions and work collaboratively with cross-functional teams for the delivery of technical source documents in accordance with project timelines.
  • Author and/or review compliant RA MD documentation for HA submissions, applying agreed RA MD Global regulatory strategies, current regulatory standards and guidelines.
  • Lead, prepare and communicate RA MD risk management assessments, contingency plans, and lessons learned on major submissions and escalate as appropriate.
  • Facilitate/support device related interactions with Health Authorities globally.
  • Contribute to knowledge sharing, e.g. provide coaching within RA CMC and other functional areas.
  • Contribute to the development of new guidance, policy, and processes.

Requirements

  • Experience in Medical Device Regulatory Affairs.
  • Significant experience in the combination product or medical device industry.
  • Proven knowledge of regulatory submission and approval processes for medical devices and combination products.
  • Ability to critically evaluate data across diverse scientific disciplines.
  • Understanding of product development and lifecycle management.
  • Demonstrated success in leading and prioritizing multiple projects in global, cross-functional teams.
  • Strong independent working skills with the ability to manage timelines and workload effectively.
  • Excellent planning, organizational, and interpersonal skills.
  • Proficiency in computer and IT systems.

Benefits

  • Commitment to Diversity & Inclusion

Job title

Associate Director, Regulatory Affairs – Medical Devices

Job type

Experience level

Senior

Salary

Not specified

Degree requirement

Bachelor's Degree

Location requirements

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