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 to apply. You may just be the right candidate for this or other roles.

Benefits at Viatris

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. Some of our benefits include the following on top of a competitive salary:

Excellent career progression opportunities
Work-life balance initiatives
Bonus scheme
Health insurance
Pension

Diversity & Inclusion at Viatris

At Viatris, diversity and inclusion are essential to our mission. The diversity we foster in all aspects of our business can be one of our greatest strengths in redefining healthcare not as it is, but as it should be. If you would like to know more about what diversity, equity and inclusion means to us, please visit https://www.viatris.com/en/Careers/Diversity-and-Inclusion

Sustainability at Viatris

Corporate social responsibility is fundamental to the Viatris mission. We work to advance responsible and sustainable operations and leverage our collective expertise to empower people to live healthier at every stage of life, recognizing that our actions affect the stakeholders and communities we serve. To learn more about our efforts, please visit https://www.viatris.com/en/about-us/corporate-responsibility

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.

Regulatory Affairs Manager CMC

Benefits

Job Description