What are the responsibilities and job description for the Sr Manager Regulatory Submissions position at Philip Morris International?
Be a Part of a Revolutionary Change
At PMI, we're transforming our business and building a smoke-free future. This transformation creates exciting opportunities for talented professionals to make an impact, drive innovation, and grow their careers.
Our success depends on people who are committed to our purpose and have an appetite for progress.
Your Impact
As a Senior Regulatory Writing Lead, you will lead the planning, development, and quality of high-priority regulatory documents supporting U.S. tobacco and nicotine product submissions and lifecycle obligations. You will ensure clear, accurate, and compliant communication with the FDA while partnering across PMI US and Global teams.
Key Responsibilities
Regulatory Document Authoring
Base Salary: $176,000 - $220,000
PMI Offers a Competitive Compensation Package Including
To learn more, visit www.pmi.com/us.
33649
At PMI, we're transforming our business and building a smoke-free future. This transformation creates exciting opportunities for talented professionals to make an impact, drive innovation, and grow their careers.
Our success depends on people who are committed to our purpose and have an appetite for progress.
Your Impact
As a Senior Regulatory Writing Lead, you will lead the planning, development, and quality of high-priority regulatory documents supporting U.S. tobacco and nicotine product submissions and lifecycle obligations. You will ensure clear, accurate, and compliant communication with the FDA while partnering across PMI US and Global teams.
Key Responsibilities
Regulatory Document Authoring
- Author and manage FDA submissions, including PMTAs, MRTPAs, amendments, supplements, post-market reports, and responses to FDA requests.
- Prepare supporting regulatory documentation while ensuring scientific accuracy, consistency, and traceability.
- Ensure compliance with applicable FDA regulations, guidance, and company policies.
- Translate complex scientific information into compelling regulatory narratives.
- Collaborate with scientific and technical experts to identify and integrate the data needed to support regulatory submissions.
- Support regulatory strategies that enable product commercialization.
- Identify and resolve issues that could impact submission readiness.
- Serve as a regulatory subject matter expert on cross-functional project teams and monitor evolving regulatory requirements.
- 8 years of regulatory affairs experience in tobacco, pharmaceuticals, or other FDA-regulated industries.
- 5 years of regulatory/scientific writing experience or evaluation of FDA applications for tobacco products.
- Demonstrated leadership in complex regulatory writing projects and cross-functional content integration.
- Strong knowledge of FDA tobacco product regulations and submission requirements.
- Expertise in FDA premarket applications, post-market reporting, and CTP processes.
- Exceptional writing, editing, and communication skills.
- Advanced scientific degree (PhD, ScD, PharmD, MS, MPH, or equivalent) preferred.
Base Salary: $176,000 - $220,000
PMI Offers a Competitive Compensation Package Including
- Annual bonus eligibility
- Medical, dental, and vision coverage
- 401(k) with company match
- Generous PTO
- Wellness, commuter, and pet insurance benefits
- Smart Work hybrid flexibility
- Shape the future of a smoke-free world.
- Work alongside talented global colleagues.
- Grow within a large, international organization.
- Join an inclusive culture where everyone's contributions are valued.
To learn more, visit www.pmi.com/us.
33649
Salary : $176,000 - $220,000