Manager Regulatory CMC Sciences (Injectables)

Mylan Teoranta 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 Every day, we rise to the challenge to make a difference and here’s how the   role will make an impact: Develop and implement global CMC regulatory strategies for injectable products. Interpret and communicate regulatory requirements and provide risk-based regulatory guidance to stakeholders. Prepare, review and analyse global CMC submission documentation and lifecycle management activities. Support manufacturing sites with regulatory strategies and documentation for variations and supplements. Ensure regulatory compliance through effective management of CMC activities and change controls. Collaborate with regional regulatory, labelling, quality, supply chain and manufacturing teams to support submissions and agency interactions. Provide responses to health authority queries and participate in regulatory authority meetings and inspections as required. Act as a regulatory subject matter expert within cross-functional project teams. Mentor colleagues and contribute to knowledge sharing and capability development. Maintain awareness of emerging regulatory requirements and industry trends, communicating impacts to relevant stakeholders.              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: Bachelor's degree (or equivalent) in a science-related discipline. Experience working within Regulatory Affairs in the pharmaceutical industry. Hands-on experience authoring post-approval CMC lifecycle management submissions. Hands-on Regulatory CMC experience supporting injectable products. Strong knowledge of global regulatory requirements, particularly US regulations. Experience with injectable, parenteral or combination product submissions. Excellent written and verbal communication skills, including preparation and review of regulatory documentation. Strong understanding of cGMP requirements, CFR, USP, Ph. Eur. and FDA guidance. Experience collaborating across Regulatory Affairs, Manufacturing, Supply Chain, Quality, Commercial, Medical and Legal functions. Proficiency with Microsoft Office applications and regulatory systems such as TrackWise and Documentum. Strong project management skills and the ability to deliver to time, cost and quality standards. Previous people management experience would be advantageous. TOPRA certification or RAC qualification preferred. At Viatris, we are dedicated to building a truly diverse, inclusive and authentic workplace, so if you’re excited about this role but your past experience doesn’t fully align with every requirement, we still encourage you to apply. You may just be the right candidate for this or