Director Regulatory CMC Sciences Project Management

Viatris; Dublin; On-site; EUR 150,000 - 190,000; Full time

Benefits offered by this job

Excellent career progression

Work-life balance initiatives

Bonus scheme

Health insurance

Pension

Job summary

Viatris is seeking a Director Regulatory CMC Sciences Project Management in Ireland to lead global, complex post-approval change programs and site transfers. You will drive regulatory strategy, coordinate cross-functional teams, and manage large-scale projects from planning to submission.

The role requires hands-on CMC authoring and strong leadership within a matrixed organization. Join Viatris to contribute to global healthcare access, with opportunities for mentorship, dashboards of regulatory

Qualifications

• Hands-on CMC authoring experience (registrations or post-approval variations).
• Proven capability in managing complex regulatory projects with PM tools.
• Extensive knowledge of post-approval variations for site transfers and alternate API sourcing.
• Knowledge of current and emerging regulatory requirements and global submission expectations.

Responsibilities

• Provide regulatory project management for global, large-scale, complex network projects.
• Coordinate priorities across multiple projects; develop tools for submission planning and forecasting timing.
• Lead team oversight for contracted GRA resources.
• Collaborate with Ops, R&D, Quality, Sourcing to guide regulatory assessments for site transfers and sourcing.
• Develop and maintain regulatory strategies and mitigation plans.
• Create dashboards and metrics for stakeholder reporting.
• Serve as the internal single point of contact for a broad project portfolio.

Skills

Regulatory project management

Regulatory strategy

Communication skills (written & oral)

Cross-functional collaboration

Leadership of matrixed teams

Submission planning & forecasting

Stakeholder management

Problem solving / risk mitigation

Strategic thinking

Mentoring colleagues

Tools

Microsoft Office Suite

Documentum-based applications

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.

The Role & What You Will Be Doing

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

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

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 offercompetitivesalaries, benefitsandan 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.