Senior Specialist Regulatory Key Initiatives
ViatrisDublin, Ireland
Posted April 3, 2026
Full Time
About the Company
Viatris Inc. (NASDAQ: VTRS) 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. In 2022 alone, we supplied high-quality medicines to approximately 1 billion patients around the world. With our exceptionally extensive and diverse portfolio of medicines, a one-of-a-kind global supply chain designed to reach more people when and where they need them, and the scientific expertise to address some of the world’s most enduring health challenges, access takes on deep meaning at Viatris. We have the ability to touch all of life’s moments, from birth to end of life, acute conditions to chronic diseases. We are headquartered in the U.S., with global centers in Pittsburgh, Shanghai and Hyderabad, India Social Media Guidelines: https://newsroom.viatris.com/social-media-community-guidelines Investors: https://investor.viatris.com Corporate Social Responsibility: https://www.viatris.com/sustainability Connect with Viatris Instagram: https://www.instagram.com/viatrisinc X: https://www.x.com/viatrisinc Viatris and our recruiting firms will not ask for sensitive personal information, such as your social security number, date of birth or bank account details via text, email or social media. Additionally, Viatris representatives do not request payment or personal bank information nor send payment to purchase hardware on your own. Viatris.com is the primary source of all company job postings and authorized third-party career websites.
Job Description
Viatris is a global healthcare company looking for a Senior Specialist Regulatory Key Initiatives to monitor and interpret global regulatory initiatives, with a focus on EU regulations, and ensure the organisation remains compliant and informed. The role will lead cross-functional collaboration, drive data management and enrichment activities, and support system and process improvements within RIM and related platforms.
Requirements
- Bachelor's degree in pharmaceutical industry experience, preferably in Regulatory Affairs or Regulatory Operations
- Strong knowledge of EU regulatory frameworks, including EMA procedures, XEVMPD, and working knowledge of IDMP and SPOR
- Experience with Regulatory Information Management (RIM) systems and understanding of the eCTD structure
- Strong organisational skills, with the ability to manage multiple projects and deadlines simultaneously
- Comfort working with complex systems and IT tools, including document and data management platforms
- Excellent attention to detail and a proactive, continuous learning mindset
- Strong collaboration and communication skills, with the ability to work cross-functionally and present complex information clearly
- Proficiency in Microsoft Word and Excel; experience with document management systems is advantageous
Benefits
- Competitive salary
- Benefits
- Inclusive environment
- Excellent career progression opportunities
- Work-life balance initiatives
- Bonus scheme
- Health insurance
- Pension