Senior Manager, Regulatory Science CMC Complex

Viatris; Dublin; On-site; EUR 90,000 - 150,000; Full time

Benefits offered by this job

Excellent career progression

Work‑life balance

Bonus scheme

Health insurance

Pension

Job summary

McDermott Laboratories Limited, a Viatris affiliate, seeks a senior CMC regulatory professional to lead global regulatory strategies for complex products. You will coordinate submissions, work with R&D, Quality, and Regulatory Affairs, and guide teams through lifecycle projects in a fast-paced global setting.

The role emphasizes science-based decision making, risk management, and engagement with health authorities to ensure timely approvals and lifecycle success.

Qualifications

• Bachelor's degree in a scientific discipline required; Master's degree preferred.
• Significant pharmaceutical industry experience, including regulatory affairs 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, and lifecycle management.

Responsibilities

• Develop and execute global CMC regulatory strategies for complex products across development and lifecycle.
• Assess CMC regulatory requirements, identify risks, and develop mitigation strategies for regulatory success.
• Prepare, coordinate, and deliver high-quality global CMC regulatory submissions (registrations, changes, renewals).
• Support Global Regulatory Leads or act as the Global Regulatory Lead for products/projects.
• Serve as CMC regulatory SME on cross-functional teams with R&D, Quality, Regulatory Affairs and regional stakeholders.
• Manage regulatory commitments, submission timelines, agency interactions, and regulatory intelligence.

Skills

Communication skills

Project management

Regulatory knowledge

Problem solving

Scientific judgment

MS Office

Regulatory submissions

Education

Bachelor's degree in science

Master's degree preferred

Tools

Regulatory document management systems

MS Office

Job description

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

• 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 contributing to regulatory strategy development.
• Excellent written and verbal communication skills with the ability to communicate effectively across all levels of an organization.
• Demonstrated project management skills and ability to manage multiple priorities in a fast‑paced, global environment.
• Strong business acumen, problem‑solving capabilities, and sound scientific judgment.
• Proficiency with Microsoft Office applications and regulatory document management systems.

At Viatris, we are dedicated to building a truly diverse, inclusive and authentic workplace, so if you’re excited about this role but your past experience doesn’t fully align with every requirement, we still encourage you to apply. You may just be the right candidate for this or other roles.

Benefits At Viatris

• Excellent career progression opportunities
• Work‑life balance initiatives
• Bonus scheme
• Health insurance
• Pension

Diversity & Inclusion at Viatris

At Viatris, diversity and inclusion are essential to our mission. The diversity we foster in all aspects of our business can be one of our greatest strengths in redefining healthcare not as it is, but as it should be. If you would like to know more about what diversity, equity and inclusion means to us, please visit https://www.viatris.com/en/Careers/Diversity-and-Inclusion

Sustainability at Viatris

Corporate social responsibility is fundamental to the Viatris mission. We work to advance responsible and sustainable operations and leverage our collective expertise to empower people to live healthier at every stage of life, recognizing that our actions affect the stakeholders and communities we serve. To learn more about our efforts, please visit https://www.viatris.com/en/about-us/corporate-responsibility

At Viatris, we offer competitive salaries, benefits and an inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others.

Viatris is an Equal Opportunity Employer.