Director Regulatory CMC Sciences Project Management

1100 Mylan Pharmaceuticals Inc.; Dublin; On-site; EUR 150,000 - 210,000; Full time

Benefits offered by this job

Health insurance

Bonus scheme

Pension

Job summary

Viatris invites an experienced Director to lead regulatory CMC project management across global networks, focusing on large-scale site transfers and alternate API sourcing. You will coordinate multi-project priorities, mentor teams, and deliver robust submission packages with clear risk mitigation.

Advanced knowledge of post-approval variations, cGMPs, and regulatory strategies is essential, as is collaboration with senior stakeholders to drive timely, compliant outcomes.

Qualifications

• Hands-on CMC authoring experience (registrations or variations).
• Proven ability to manage complex regulatory projects.
• Strong knowledge of post-approval variations and site transfers.

Responsibilities

• Manage global, large-scale regulatory projects and site transfers.
• Coordinate priorities across multiple projects and teams.
• Develop submission plans, tracking, and timing forecasts.
• Lead contracted GRA resources and mentor colleagues.
• Communicate regulatory risks and mitigation progress.
• Generate dashboards and metrics for stakeholders.

Skills

Regulatory project management

CMC authoring

Cross-functional leadership

Stakeholder management

Dashboarding / reporting

Education

Bachelor’s or Master’s in life sciences

Tools

Microsoft Office

Documentum

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

The Director Reg. CMC Sciences Project Management is an emerging senior level position, recognized as a regulatory expert in the management of global and complex post-approval changes. The position is primarily devoted to the project management of large-scale and complex manufacturing site transfers and alternate API sourcing activities, impacting Viatris internal sites and CMOs largely across the core, complex and established brands product portfolios.

Every day, we rise to the challenge to make a difference and here's how the Director Regulatory CMC Sciences Project Management role will make an impact: For this role, we’re looking for a candidate who has an effective combination of the following qualifications, skills and experiences:

• Provides regulatory project management support for global, large-scale and complex network optimization projects
• Serves as a matrixed manager to coordinate and align on priorities across multiple projects, developing and maintaining tools for submission planning, tracking and forecasting best/base approval timing to enable accuracy for supply continuity planning to minimize stock-outs.
• Provides team leader oversight for all contracted GRA resources
• Cultivates sustainable and effective relationships across multiple internal stakeholders (e.g., Ops, R&D, Quality, Sourcing) to drive global regulatory assessments for site transfers and alternate sourcing activities, predicated on robust gap assessments and regulatory strategies, and right-first-time submission packages.
• Assesses and communicates regulatory risks, and develops and tracks progress of mitigation plans.
• Uses technical and scientific knowledge in support of submission preparation and review, and assures regulatory compliance through the appropriate use of Change Control, external and internal regulatory requirements, and maintenance of Viatris’ regulatory systems.
• Presents and articulates issues for resolution, communicating regularly with key stakeholders to ensure alignment, providing consultation as a scientific/technical resource within the department/cross-functional and therapeutic teams for assigned projects, mentoring and sharing experience with colleagues.
• Develops dashboards and metrics for reporting to stakeholders.
• Position is expected to serve as the single Point of Contact internally across a large portfolio of projects, and manage up to 20+ ETW resources across a matrixed and global organization.

About Your Skills & Experience

Knowledge: Mandatory hands-on CMC authoring experience (initial registrations or post-approval variations) – generalist knowledge across global regulatory affairs disciplines.

Proven capability in managing complex Regulatory projects and use of project management tools.

Extensive knowledge of post-approval variations specific to site transfers and alternate API sourcing, and of cGMP’s to assess technical, scientific & regulatory merits of regulatory information, commitments and data to lead teams and/or complex projects.

Extensive technical, functional, and industry knowledge in shaping project strategy, reducing regulatory burden & improving regulatory flexibility across global markets and diverse therapeutic areas.

Independently capable of executing activities related to complex projects across the commercial manufacturing product lifecycle.

Advanced understanding of current and emerging regulatory requirements & expectations, criteria for submission & approval globally.

Possesses sound understanding of business expectations, with proven ability to partner successfully with GRA leadership and other senior stakeholders in achieving objectives.

Skills & Abilities

• Advanced skills in written & oral communications (mandatory).
• Computer literacy with Microsoft Office Suite and Documentum-based applications.
• Prior experience managing projects and matrixed teams and/or serving as a people manager.
• Advanced knowledge of global regulatory requirements.
• Demonstrated commitment & dedication to scientific & regulatory integrity & quality compliance.
• Ability to engage in the external regulatory and pharmaceutical environment.
• Proven ability to deliver to time, cost and quality standards.
• Demonstrated strategic thinking and ability to integrate strategies into actionable plans.
• Demonstrated experience serving as a Subject Matter Expert in specific relevant disciplines or as a recognized resource for specific pharmaceutical science projects and/or specialized expert in specific regulatory domains.

Benefits at Viatris

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.

Some of our benefits include the following on top of a competitive salary:

• 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. Viatris is a global healthcare company formed in 2020 through the combination of Mylan and Upjohn, a legacy division of Pfizer. By integrating the strengths of these two companies, including our global workforce, we aim to deliver increased access to affordable, quality medicines for patients worldwide, regardless of geography or circumstance. We believe in healthcare as it should be – empowering people worldwide to live healthier at every stage of life. Because of our unwavering belief that better access leads to better health, we leverage our best-in-class manufacturing and scientific expertise and proven commercial capabilities to bring quality medicines to patients when and where they need them.