Senior Drug Safety Physician (m/f/d)

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VIATRIS INNOVATION GMBH 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 At Viatris Innovation GmbH, we are engaged in the development of innovative drug products to treat unmet medical needs. This is an exciting role where you will act as both Subject Matter Expert and strategic Safety Lead, working across different therapeutic areas and clinical phases. If you thrive on scientific integrity and objectivity, ownership, and cross-functional collaboration , this could be your next step. Lead medical safety oversight for assigned clinical development programs Drive signal detection, evaluation, and risk management strategies Act as chair and medical lead for the Safety Management Team (SMT) Present safety insights and recommendations to the Drug Safety Committee Contribute to key regulatory deliverables such as DSURs, RMPs, ISS, and Investigator Brochures Collaborate closely with clinical, regulatory, and data management teams Represent Viatris in interactions with Health Authorities and external committees Provide expert individual case medical review of SAEs and ensure accurate safety reporting 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: Medical degree (MD or equivalent) 7+ years of experience in pharmacovigilance, clinical safety, or clinical development Strong expertise in drug safety regulations, GCP, and global PV requirements Proven ability to interpret complex clinical safety data and drive decisions Experience with regulatory safety documents (e.g., DSUR, RMP, CCDS) Excellent communication and presentation skills in English (advanced level required)

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