Head of US Regulatory Affairs Advertising and Promotion, Global Regulatory Affairs

Mylan Pharmaceuticals Inc.

Viatris is a global healthcare company uniquely positioned to bridge the traditional divide between generics and brands, combining the best of both to more holistically address healthcare needs globally. With a mission to empower people worldwide to live healthier at every stage of life, we provide access at scale, currently supplying high-quality medicines to approximately 1 billion patients around the world annually and touching all of life's moments, from birth to the end of life, acute conditions to chronic diseases.

We have been included on number of award lists that demonstrate the impact we are making.

Every day, we rise to the challenge to make a difference and here’s how the role will make an impact:

• Develop and implement A&P regulatory strategies; establish and maintain local policies, SOPs, and compliance frameworks aligned with global practices ensuring consistent, risk-based decision-making across all promotional activities.
• Partner with medical affairs, legal, marketing, and commercial teams to ensure promotional materials (e.g., physician/patient sales, marketing, educational materials, press releases) are accurate, balanced, substantiated and aligned with overall brand strategy and business objectives.
• Serve as the primary contact with the FDA's Office of Prescription Drug Promotion (OPDP) within the U.S. Food and Drug Administration; lead submissions, risk mitigation strategies, and regulatory interactions including advisory comments, Form FDA 2253 submissions, and responses to regulatory enforcement actions.
• Review and approve promotional materials for completeness, accuracy, and consistency with approved labeling; assess clinical evidence supporting claims.
• Build a best-in-class A&P local function with efficient, compliant review and execution processes including optimization of MLR/PRC review workflows and continuous process improvement initiatives.
• Management of a 4–5-member team including coaching, performance management, and capability development.
• Monitor FDA, FTC, and SEC enforcement trends and communicate risks to senior leadership, translating external insights into proactive guidance and risk mitigation strategies for the business.
• Maintain relationship with Global Head of Labeling, Advertising & Promotion to ensure consistency across regions.

• Minimum of a bachelor’s degree (or equivalent) and relevant industry experience required. A degree in scientific discipline is strongly preferred. An advanced degree (MS, PharmD, MD) in a scientific discipline is a plus, A minimum of 10 years of experience in Regulatory Affairs with at least 5 years subject matter expertise as strategic leader in Ad Promo. Related experience and/or education may be considered.
• Must possess expert knowledge of regulatory guidance pertaining to advertising and promotion for pharmaceutical products. Strong knowledge of regulatory environment and FDA.
• Deep knowledge of FDA promotional regulations, guidance, and enforcement trends.
• Strong cross‑functional collaboration and stakeholder management skills.
• Expertise in promotional review processes (e.g., PSMR – Promotional Submission Management Review).
• Ability to lead regulatory committees and influence business strategy.
• Experience with medical, scientific, and promotional materials compliance.
• Strong communication and presentation skills for internal and external audiences.
• Must possess excellent analytical, written and verbal communication, interpersonal, and project management skills.
• Must possess a strong work ethic and have outstanding organization and time management skills. Must have strong computer skills and be proficient within the…