Find Senior manager, regulatory affairs cmc Jobs in Balbriggan, D

Senior Manager, Regulatory Affairs CMC
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- Employee discount
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DHS Complete Hire - Drogheda Branch and other sites —Drogheda, County Louth
- €55,000–€65,000 a year
- Full-time
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- Microsoft Office
- Organisational skills
- Wellness program
Quick apply
6d
Senior Manager, Global Regulatory Affairs – Business Process
Viatris —Northern Cross, County Dublin
- Full-time
- Project management
- No degree
Senior National Account Manager
Primeline Group —Ashbourne, County Meath
- Full-time
- Sales
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- Analysis skills
Quick apply
Quality Operations Manager
PCI Pharma Services —Stamullin, County Meath
- Full-time
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Senior Regulatory Affairs Officer (12 Month FTC)
Viatris —Northern Cross, County Dublin
- Full-time
- Bachelor's degree
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Ramboll —Swords, County Dublin
- Full-time
- Hybrid work
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Director Regulatory Affairs Global CMC
Viatris —Northern Cross, County Dublin
- Full-time
- Project management
- Mentoring
- Manufacturing
Senior Manager
Xeinadin —North Dublin, County Dublin
- Communication skills
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5d
Senior Site Reliability & Maintenance Manager
Mondelēz International —Coolock, County Dublin
- Full-time
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Senior Manager, Global Device Quality
Viatris —Northern Cross, County Dublin
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Senior Manager, Device Program Lead
Viatris —Northern Cross, County Dublin
- Full-time
- Project management
- Leadership
Manager, Automation Engineering
PCI Pharma Services —Stamullin, County Meath
- Full-time
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Contract Project Manager
WaterWipes —Drogheda, County Louth
- Engineering
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5d
Standard Confectionary Lead - Senior Brand Manager
Mondelēz International —Coolock, County Dublin
- Full-time
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Senior Manager, Core Labelling Strategy
Viatris —Northern Cross, County Dublin
- Full-time
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Business Support Manager
Kare Plan Ltd —Kilbarrack, County Dublin
- €50,000 a year
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- Microsoft Excel
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- Supervising experience
Quick apply
15h
Project Manager (Construction)
Techrete UK & Ireland —Balbriggan, County Dublin
- Full-time
- Microsoft Excel
- Engineering
- Analysis skills
Quick apply
Director Regulatory CMC Sciences Project Management
Viatris —Northern Cross, County Dublin
- Full-time
- Microsoft Office
- Project management
- Mentoring

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Senior Manager, Regulatory Affairs CMC

Viatris -
Northern Cross, County Dublin

Apply Now

Job details

Full-time

Qualifications

Microsoft Office
Project management

Full job description

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 Senior Manager Global Branded CMC Strategy possesses CMC regulatory knowledge and quality expertise to independently prepare regulatory assessments & contribute to global regulatory strategies for projects across all aspects of drug development or manufacturing lifecycle and works to support the Upjohn portfolio.

Every day, we rise to the challenge to make a difference and here’s how the Senior Manager, Regulatory Affairs role will make an impact:

Ensure global regulatory compliance with external requirements and internal quality procedures across all markets.
Apply sound regulatory judgment, strategic thinking, and business acumen to develop and implement global regulatory strategies.
Prepare, review, and deliver high-quality CMC submissions for new registrations, post-approval changes, renewals, and responses to agency queries.
Lead CMC activities for assigned projects, including submission planning, risk assessment, and regulatory timelines tracking.
Represent CMC on cross-functional project teams, ensuring alignment with scientific, technical, and regulatory criteria.
Maintain up-to-date regulatory documentation and systems, manage commitments, and ensure submission compliance.
Collaborate effectively with internal and external stakeholders, including Regulatory, Quality, R&D, and global/regional teams.
Serve as a technical and scientific resource for complex regulatory issues and provide mentoring to colleagues.
Support implementation of regulatory policies, procedures, and continuous improvement initiatives across CMC functions.
Build and maintain professional relationships with regulatory authorities and industry bodies to enhance regulatory success.
Contribute to CMC-related projects, training, and development programs, while modeling Viatris’ values and behaviors.
Participate in external forums, trade groups, or industry conferences relevant to CMC functions as needed.

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:

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 cGMP’s required to assess technical, scientific and regulatory merits of CMC information, commitments and data to lead teams and/or project(s).
Advanced technical, functional, and industry knowledge to shape strategic direction of assigned project(s), reduce regulatory burden and improve regulatory flexibility commensurate with business needs.
Advanced knowledge of regulatory requirements and expectations, criteria for submission and approval globally and experience of interactions with regulatory authorities for projects.
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.

Advanced skills in written & oral communications (mandatory).
Computer literacy with Microsoft Office Suite and Documentum-based applications.
Project Management skills
Ability to engage in the external regulatory and pharmaceutical environment.
Some experience serving as a Subject Matter Expert in specific relevant disciplines or as a resource for specific pharmaceutical science projects in specific regulatory domain(s).

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.

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 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.

Apply Now

Refine Your Search

senior manager, regulatory affairs cmc jobs in balbriggan, d

Senior Manager, Regulatory Affairs CMC

Senior National Account Manager

Transport Manager / Senior Transport Coordinator

Senior Manager, Global Regulatory Affairs – Business Process

Senior National Account Manager

Quality Operations Manager

Senior Regulatory Affairs Officer (12 Month FTC)

Senior Project Manager

Director Regulatory Affairs Global CMC

Senior Manager

Senior Site Reliability & Maintenance Manager

Senior Manager, Global Device Quality

Senior Manager, Device Program Lead

Manager, Automation Engineering

Contract Project Manager

Standard Confectionary Lead - Senior Brand Manager

Senior Manager, Core Labelling Strategy

Business Support Manager

Project Manager (Construction)

Director Regulatory CMC Sciences Project Management

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