Head of Global Regulatory CMC Sciences – (Based Anywhere in Europe)
Viatris is seeking a senior leader for our global CMC regulatory team.
The role will shape strategic regulatory approaches, lead a diverse global team, and collaborate cross‑functionally to expedite the regulatory lifecycle for branded and generics.
Key Responsibilities
Provide strategic leadership and direction for the global CMC regulatory team across all branded, second brand, and authorized generic formulations.
Establish and maintain strong partnerships with cross‑functional stakeholders (R&D, Quality, Technical Services, Operations, Commercial & Medical) to develop and implement CMC registration strategies that expedite product launch and lifecycle maintenance.
Provide input on new business development opportunities and support development of local regulatory agency relationships.
Assure consistent standards and processes throughout the global CMC regulatory teams, aligning with regulatory policies, global policies, and corporate leadership priorities.
Collaborate with Global, Regional and Local Regulatory, R&D, Technical Services, Clinical Development/Medical Affairs, and Commercial to develop harmonized filing strategies and engage key stakeholders.
Lead change management and continuous improvement projects, capturing best practices and incorporating them into future regulatory strategies.
Oversee performance management, talent acquisition, and succession planning for the global CMC team, ensuring professional growth and development.
Represent Viatris at global health authorities, fostering engagement and advancing future CMC regulatory initiatives.
Qualifications & Experience
Higher degree (MS, Ph D, Pharm D, MBA) preferred.
Advanced global CMC leadership experience with deep technical and business expertise across the drug development and commercial lifecycle.
Experience across product development lifecycle for products in key geographies, including leadership for complex and innovative approvals.
Experience with branded and generic regulatory submissions, DMFs, CEP filings, and global compendial requirements.
Line management and senior-level leadership experience essential.
Demonstrated delivery in a complex matrix environment, with strong stakeholder management and cross‑functional collaboration.
Proven ability to partner with Regulatory, Manufacturing, Quality, Safety, Medical, Commercial, Legal, and senior stakeholders to achieve objectives.
Strong understanding of pharmaceutical development and impact on global business outcomes.
Benefits
Competitive salary and bonus scheme.
Health insurance and pension.
Excellent career progression opportunities.
Work‑life balance initiatives.
Closing date for applications is 2nd January 2026.
Viatris is an Equal Opportunity Employer.
We welcome applications from people of all background and identity.
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