Regulatory Affairs Manager CMC

McDermott Laboratories Limited 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 Manager, Regulatory Affairs Brands CMC will independently prepare regulatory assessments and contribute to global regulatory strategies across the drug development and manufacturing lifecycle, supporting the Upjohn product portfolio. Every day, we rise to the challenge to make a difference and here’s how the Manager, Regulatory Affairs Brands CMC role will make an impact: Ensuring regulatory conformance and consistency globally, in compliance with external regulatory requirements and internal quality procedures Developing robust regulatory strategies, leveraging technical and regulatory knowledge to mitigate risk Preparing and delivering high-quality CMC regulatory submissions and submission management plans for global regulatory agencies Serving as CMC representative on core project teams, assessing regulatory risks and shaping global regulatory strategies in line with regulatory, scientific and technical criteria Managing regulatory issues and tracking regulatory commitments and timelines across projects, products and markets with minimal supervision Authoring and/or coordinating CMC activities for new registrations, post-approval changes, renewals, annual reports and line extensions, including responses to Agency queries Acting as a technical and scientific resource, providing guidance on complex projects and mentoring colleagues within your area of expertise Building effective relationships with local and global partners across R&D, Quality, and Regulatory teams 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); a Master's degree is preferred, and a combination of education and experience will be considered Significant pharmaceutical experience (Quality, Technical Services or R&D), including a number of years of pharmaceutical regulatory experience Hands-on CMC authoring experience (initial registrations or post-approval variations) Solid understanding of development and commercial activities and cGMPs required to assess the technical, scientific and regulatory merits of CMC information Advanced written and oral communication skills Prior experience managing projects, with computer literacy in Microsoft Office Suite and Documentum-based applications Ability to work autonomously with minimal supervision, exercising independent judgment on complex, non-standardized problems 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