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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. This posting supports ongoing hiring needs and may be used to consider candidates for upcoming opportunities. 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 a number of award lists that demonstrate the impact we are making. Every day, we rise to the challenge to make a difference, and here’s how the Senior Regulatory Affairs Manager - Central Regulatory Affairs (CRA), Europe role will make an impact: Key responsibilities for this role include: Leadership & People Development Lead a high-performing team of Regulatory professionals overseeing a portfolio of products developed internally, externally (in partnership with Viatris) or via a Third Party/ Business Development (BD) Partner, ensuring successful product lifecycle management and alignment with global business goals. Provide guidance and mentorship to ensure effective execution of regulatory strategies. Regulatory Strategy Overall regulatory responsibility for all Regulatory activities impacting European markets for a diverse portfolio of medicinal products (and/or other product classifications) including Generic, Established Brand, Innovative, and Value-Added products. Oversee regulatory compliance to ensure portfolio of products meet all legal and industry standards. Manage a portfolio of products developed internally, externally (in partnership with Viatris) or via a Third Party/ Business Development (BD) Partner. Responsible for the development and implementation of European regulatory strategy that aligns with Global Regulatory Affairs objectives, partnering with Global Regulatory Affairs workstreams, maintain relations with internal/ external strategic partners through to stakeholders, provide regulatory guidance to other business functions, as well as Local European Regulatory Teams. Responsible for ensuring on-time submission of post-approval lifecycle activities, to include: Renewals, Variations (Administrative, CMC, Safety), Article 61(3) notifications and Country-specific notifications. Portfolio Oversight Maintain procedure oversight, lead and manage new product registrations through the Centralised Procedure (CP), Decentralised Procedure (DCP), Mutual Recognition Procedure (MRP), and National pathways, serving as the primary regional expert for these procedures. Provide Submission Strategic input, define and implement robust European registration strategies to ensure commercially successful product launches and rapid market access. Partner with Local Affiliate teams to ensure CRA are appropriately educated and trained in the preparation and management of country-specific National activities; ensure timely submission and execution of agreed filing strategies for Nationally-approved portfolio. Partnership/ Communication Work closely with internal departments such as Clinical, Quality Assurance, Legal, and Commercial teams to integrate regulatory requirements into business operations and product development. Liaise closely with internal functional areas to ensure alignment in all initiatives: Business Development, Regulatory CMC Sciences, Labelling, Pharmacovigilance, Product Launch, Artwork, Supply Chain and Quality colleagues. Liaise with Third Party/ Business Development (BD) Partners, establish effective communication channels and build positive relationships in order to progress regulatory activities. Health Authority Engagement Serve as a primary liaison with regulatory authorities (e.g. European Medicines Agency (EMA), national competent authorities), leading meetings, preparing submissions, and facilitating approvals for new products or changes to existing products. Governance, Compliance & Risk Management Anticipate changes in regulations, assess their impact on operations, and develop risk mitigation strategies in collaboration with Line Manager. Investigate promptly, escalate and agree mitigation plan for any reported non-compliance issues. Business & Industry Leadership Be actively involved in due diligence activities including evaluation of regulatory strategy, launch timelines, evaluation of risks and regulatory costs. Represent the company at industry associations, conferences, external working groups, and senior executive and cross-functional leadership meetings. 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: University degree (Pharmacy, Biotechnology, and/or other Pharma/Medical scientific background) Masters in RA is preferred Fluent English - speaking and writing 10+ years RA Experience, including 2-3 years of People Management Excellent interpersonal skills 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. All qualified applicants will receive consideration for employment without regard to race, national origin, religion, age, color, sex, sexual orientation, gender identity, gender expression, disability, or protected veteran status, or any other characteristic protected by local, state, or federal laws, rules, or regulations. 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 whose mission is to empower people worldwide to live healthier at every stage of life. We meet the needs of patients around the world by acting decisively with ingenuity and resolve. Whether we're developing new medicines, working to maintain a resilient supply of needed therapies, or pursuing bold innovation, we strive to deliver solutions that are effective at scale and built to endure. We're purpose-built to make an impact with a broad portfolio that spans generics, value-added medicines, established brands, and innovative medicines that address areas of significant unmet need. We are headquartered in the U.S., with global centers in Pittsburgh, Shanghai, and Hyderabad, India. 
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viatris
Lisbon-Office-Parque das Nacoes, Portugal
Senior Regulatory Affairs Manager - Central Regulatory Affairs (CRA), Europe.
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