Senior Specialist Regulatory Operations and System Support

Mylan, Lda. 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 Senior Specialist Regulatory Operations and System Support will support the coordination and management of regulatory documentation and XEVMPD/IDMP submissions to health authorities. Working closely with the central organisation and local affiliates, the role involves tracking registration activities, managing submission status reporting, and ensuring both internal business needs and regulatory authority requirements are met. The successful candidate will also contribute to regulatory systems projects aimed at driving efficiency and effectiveness, while supporting broader project management activities under the direction of the project lead. Every day, we rise to the challenge to make a difference and here’s how the Senior Specialist Regulatory Operations and System Support role will make an impact: Maintain xEVMPD (Article 57) data utilising XEVMPD software, ensuring data quality and compliance with submission timelines when submitting to Health Authorities. Respond to EMA and other Health Authority queries relating to xEVMPD/IDMP data in a timely and accurate manner. Provide registration tracking input in line with external and internal regulatory requirements and processes. Coordinate regular communication with MA Coordinators and/or third parties to ensure outstanding actions are completed on time and in accordance with regulatory requirements. Support XEVMPD system administration, including user management and system updates. Perform reconciliation of xEVMPD/IDMP data with affiliates as required. Monitor regulatory requirement updates and contribute to their implementation into relevant systems and processes. Manage SPOR PMS data submissions and maintain the existing product portfolio within the system.     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: Minimum of a Bachelor's degree (or equivalent) in a relevant discipline, with 2–4 years of relevant experience; a combination of education and experience will be considered. Strong knowledge of EU regulations, specifically relating to Article 57(2), SPOR, and IDMP. Proven expertise in xEVMPD data submissions, associated systems, and regulatory requirements. Experience working with Regulatory Information Management Systems (RIMS). Proficiency with Document Management Systems (DMS) and tools including Adobe Acrobat and the Microsoft Office Suite. Experience engaging with health authorities and stakeholders outside of own functional area. Demonstrated ability to work collaboratively as part of a team across multiple functions and projects. Strong time management skills with the ability to