Regulatory Affairs Manager CMC (Global) â Based Anywhere in Europe
Regulatory Affairs Manager CMC (Global) â Based Anywhere in Europe
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Job Description
At VIATRIS we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs.
Viatris empowers people worldwide to live healthier at every stage of life.
We do so via:
Access Providing high quality trusted medicines regardless of geography or circumstance;
Leadership Advancing sustainable operations and innovative solutions to improve patient health; and
Partnership Leveraging our collective expertise to connect people to products and services.
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 heres how the Regulatory Affairs Manager CMC (Global) Based Anywhere in Europe role will make an impact:
Demonstrate regulatory knowledge and experience balanced judgment crisp decision-making exemplary collaboration and business acumen i.e. regulatory strategy development regulatory submission quality investigations review of policy and quality standards
Develop robust regulatory strategies leveraging both technical and regulatory knowledge to mitigate risks.
Prepare and deliver high-quality CMC regulatory submissions & submission management plans for global regulatory agencies.
Execute using regulatory policies and operational processes for delivering the product portfolio.
Serve as CMC representative on a core project(s) manage project activities assess regulatory risks and develop plans to develop global regulatory strategies for programs in accordance with regulatory scientific and technical criteria.
Manage regulatory issues maintain submission information in relevant CMC systems track regulatory commitments & timelines for specific projects/products/markets with minimal supervision.
Present and articulate issues for resolution communicating regularly with key stakeholders to ensure alignment and providing consultation as a scientific/technical resource for assigned projects mentoring and sharing experience with colleagues.
Author and/or coordinate CMC activities for new registrations post approval changes renewals annual reports and line extensions to meet filing requirements. Coordinate and contribute to responses to Agency queries and perform quality review of regulatory CMC submissions.
Serve as a technical and scientific resource and provide guidance for completion of difficult and complex projects.
Develop effective relationships with local and global internal partners i.e. R&D; Quality; Global Country & Regional Regulatory Leads; other CMC lines.
Execute training related activities (e.g. compliance-related HR policies) and individual development plans participate in cross-disciplinary forums and learning opportunities engage in Straight Talk and Listen exchanges demonstrate and model adherence to all Viatris behaviors and values embrace and comply with Principles of Integrity.
Manage and contribute to CMC-related projects initiatives and actions.
Participate as required in pharmaceutical industry conferences or serve externally as a representative to pharmaceutical trade group advisory committees relevant to CMC functions.
About Your Skills & Experience
For this role were looking for a candidate who has an effective combination of the following qualifications skills and experiences:
Mandatory hands-on CMC authoring experience (initial registrations or post-approval variations)
Sufficient level of knowledge and solid understanding of the development and commercial activities and cGMPs required to assess technical scientific and regulatory merits of CMC information commitments and data to lead teams and/or project(s).
Technical functional and industry knowledge to shape strategic direction of assigned project(s) reduce regulatory burden and improve regulatory flexibility commensurate with business needs.
Regulatory requirements and expectations criteria for submission and approval globally and experience of interactions with regulatory authorities for projects.
Updating interpreting and applying global and regional CMC guidelines along with the ability to contribute to global regulatory strategies by proactively discussing with partners.
Emerging awareness of new scientific or manufacturing technology.
Sound understanding of business expectations across divisions
Sound understanding and advanced knowledge of the principles practices and concepts of regulatory CMC/ policy/ publishing disciplines and a working knowledge of the principles practices concepts and operations in other relevant disciplines.
At Viatris we are dedicated to building a truly diverse inclusive and authentic workplace so if youre excited about this role but your past experience doesnt fully align with every requirement we still encourage you to apply. You may just be the right candidate for this or other roles.
Why 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. You will also have the opportunity to access excellent career progression opportunities and work-life balance initiatives.
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 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 Viatris we offercompetitivesalaries benefitsandan 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.
Required Experience:
Exec
Employment Type
Full-Time
