Work Flexibility: Hybrid or Onsite

Key Areas of Responsibility:

• Develops and implements processes involved with maintaining annual licenses, registrations, and listings
• Reviews and approves advertising and promotion to ensure regulatory compliance
• Assures post-market regulatory requirements are met (e.g. required reports, supplemental submissions and other post-marketing commitments)
• Submits notifiable changes and supplemental dossiers to the appropriate regulatory authorities to update product information and/or instructions for use to reflect current state of product knowledge
• Participates in implementation of regulatory strategy and processes for handling recalls and communication to stakeholders (e.g. HCP, patient, distributor, and health authorities)
• Reports product safety issues to regulatory authorities as required, to comply with local, regional, and global regulations
• Provides required information in support of product reimbursement requests
• Provides regulatory input and appropriate follow-up for inspections and audits
• Assesses regulatory intelligence to assist in the development of local, regional, and global regulatory strategies
• Evaluates the regulatory environment and contributes to providing internal advice throughout the product lifecycle (e.g., concept, development, manufacturing, marketing) to ensure product compliance
• Anticipates regulatory obstacles and emerging issues throughout the product lifecycle and develops solutions
• Identifies requirements and potential obstacles for market access distribution (federal, provincial/territorial state, reimbursement, purchasing groups, etc.)
• Assists in the development of regulatory strategy and updates strategy based upon regulatory changes
• Evaluates proposed products for regulatory classification and jurisdiction
• Determines requirements (local, national, international) and options for regulatory submission, approval pathways, and compliance activities
• Provides regulatory information and guidance for product development and planning throughout the product lifecycle to the regulatory groups and others within the organization
• Compares regulatory outcomes with initial product concepts and recommends changes or refinements based on initial regulatory outcomes
• Negotiates with regulatory authorities throughout the product lifecycle
• Identifies the need for new regulatory procedures, SOPs, and participates in development and implementation
• Helps train stakeholders on current and new regulatory requirements to ensure organization-wide compliance
• Assists other departments in the development of SOPs to ensure regulatory compliance

Education / Work Experience:

• BS in Engineering, Science, or related degree; or MS in Regulatory Science
• Typically a minimum of 2 years’ experience
• MS or RAC(s) preferred

Knowledge / Competencies:

• Project management, writing, coordination, and execution of regulatory items
• Perform technical and scientific regulatory activities
• Usually works with minimum supervision, conferring with superior on unusual matters
• Assignments are broad in nature, requiring originality and ingenuity
• Has some latitude for unreviewed action or decision
• Seeks out diverse ideas, opinion, and insights and applies them in the workplace
• Connects and relates well with people who think and act differently than oneself
• Embraces scrutiny and accepts feedback as opportunity to learn and improve
• Chooses the best alternative to achieve desired outcome or effect, giving consideration to risks, tradeoffs, timing, and available resources
• Navigates the dynamics, alliances, and competing requirements of the organization or business
• Willingly accepts challenging assignments and new career opportunities that stretch and build capabilities

Travel Percentage: None