Senior Manager, Regulatory Science CMC Complex

McDermott Laboratories Limited 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. Our global portfolio includes best-in-class, iconic brand-name products as well as global key brands; generics, including branded and complex generics; and other offerings across a wide range of therapeutic areas. We are committed to helping create healthier communities worldwide through education, outreach and better access to treatment.

For those driven to live their lives with purpose, Viatris helps employees realise their full potential by creating a collaborative culture that fosters courage and resilience. Viatris is more than just a place to work. This is a place to make a difference in the world. The Role & What You Will Be Doing Every day, we rise to the challenge to make a difference and here’s how the Senior Manager, Regulatory Science CMC Complex role will make an impact: Develop and execute global CMC regulatory strategies for complex pharmaceutical products across development and lifecycle management activities.

Independently assess CMC regulatory requirements, identify potential risks, and develop mitigation strategies to support successful regulatory outcomes. Prepare, coordinate, and deliver high-quality global CMC regulatory submissions, including new registrations, post-approval changes, renewals, annual reports, and line extensions. Support Global Regulatory Leads or act as the Global Regulatory Lead for assigned products and major regulatory projects.

Serve as the CMC regulatory representative on cross-functional project teams, partnering closely with R&D, Quality, Regulatory Affairs, Technical Operations, and regional stakeholders. Manage regulatory commitments, submission timelines, agency interactions, and regulatory intelligence activities with minimal supervision. Lead responses to health authority questions and provide quality review of complex regulatory submissions.

Act as a scientific and technical subject matter expert, providing guidance, mentorship, and regulatory leadership to colleagues and project teams. Contribute to regulatory process improvements, strategic initiatives, and high-priority business projects that support the global complex products portfolio. Build and maintain effective relationships with regulatory authorities and internal stakeholders to enhance regulatory success.

About Your Skills & Experience For this role, we’re looking for a candidate who has an effective combination of the following qualifications, skills and experiences: Bachelor's degree in a scientific discipline required; Master's degree preferred. Significant pharmaceutical industry experience, including regulatory affairs experience within CMC. Hands-on experience authoring CMC regulatory submissions for new registrations and/or post-approval variations.

Strong understanding of pharmaceutical development, manufacturing processes, cGMP requirements, and lifecycle management. Experience supporting complex dosage forms such as drug-device combinations, injectable products, respiratory products, creams, or ointments is highly desirable. Advanced knowledge of global regulatory requirements, submission pathways, and regulatory expectations. Experience supporting submissions such as NDA, ANDA, supplements, amendments, DMFs, and comparable European procedures is preferred.

Ability to interpret and apply global and regional CMC guidelines while contri