Find laboratory manager Jobs in dublin, d

Senior Manager, Regulatory Affairs CMC
Viatris —Northern Cross, County Dublin
- Full-time
- Microsoft Office
- Project management
Labelling Hub Manager (Regulatory)
Viatris —Northern Cross, County Dublin
- Full-time
- Bachelor's degree
- Communication skills
Veterinary Nurse - Small Animal
IVC —Dublin, County Dublin
- €32,000–€40,000 a year
- Full-time
- Patient care
- Communication skills
- Annual leave
- Employee assistance program
14d
RTR Manager
Abbott Laboratories —Dublin, County Dublin
- Full-time
- English
- Bachelor's degree
- Accounting
Director and Head of EMEA Emerging Biopharma Sales, IQVIA Central Laboratories
IQVIA —Dublin, County Dublin
- Full-time
- Analysis skills
- Communication skills
- Negotiation
Senior Manager, Global Regulatory Affairs – Business Process
Viatris —Northern Cross, County Dublin
- Full-time
- Project management
- No degree
Warehouse Operator
Charles River Laboratories —Dublin, County Dublin
- Full-time
- Leaving certificate
- No degree
- Organisational skills
- Annual leave
- Employee discount
Senior Systems Analyst
Abbott Laboratories —Dublin, County Dublin
- Full-time
- No degree
- IT
- Manufacturing
Building Attendant
Blackrock Health Hermitage Clinic —Lucan, County Dublin
- €33,000–€35,000 a year
- Full-time
- Forklift
- Clinic
- Communication skills
- Free parking
- Employee assistance program
Quick apply
Clinical Tutor – Histopathology
RCPI —DUBLIN 2, County Dublin
- €500 a day
- Doctoral degree
- Microsoft Office
- Master's degree
Quick apply
12d
Senior Manager, Global Device Quality
Viatris —Northern Cross, County Dublin
- Full-time
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
14d
Associate Manager, Environmental Health and Safety
Viatris —Northern Cross, County Dublin
- Full-time
- Engineering
- Bachelor's degree
- Communication skills
Director, Combination Product Development
Viatris —Northern Cross, County Dublin
- Full-time
- Engineering
- Organisational skills
- Leadership
Project Management Officer - Lead
Eurofins —Dublin, County Dublin
- Full-time
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
Quick apply
Director Regulatory CMC Sciences Project Management
Viatris —Northern Cross, County Dublin
- Full-time
- Microsoft Office
- Project management
- Mentoring
CSV Engineer (FTC 12 Months)
Takeda Pharmaceutical —Dublin, County Dublin
- €57,800–€79,420 a year
- Full-time
- Engineering
- System design
- Bachelor's degree
- Fuel card
- Employee assistance program
Materials Engineer – Bitumen & Surface Treatments
Breedon Group plc —DUBLIN 11, County Dublin
- Full-time
- Microsoft Excel
- Engineering
- Microsoft Office
- Employee assistance program
Quick apply
8d
Program Manager, Device Technical Operations ( 12 Months Agency Contract )
Viatris —Northern Cross, County Dublin
- Full-time
- Engineering
- Analysis skills
- Project management
14d
Cardiac Physiologist Senior
Blackrock Health Hermitage Clinic —Lucan, County Dublin
- Full-time
- Clinic
- Analysis skills
- Bachelor's degree
Quick apply
Staff Nurse - Endoscopy
Blackrock Health Hermitage Clinic —Dublin, County Dublin
- Full-time
- Clinic
- Communication skills
- Nursing
- Free parking
- Employee assistance program
Quick apply

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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

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

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

laboratory manager jobs in dublin, d

Senior Manager, Regulatory Affairs CMC

Labelling Hub Manager (Regulatory)

Veterinary Nurse - Small Animal

RTR Manager

Director and Head of EMEA Emerging Biopharma Sales, IQVIA Central Laboratories

Senior Manager, Global Regulatory Affairs – Business Process

Warehouse Operator

Senior Systems Analyst

Building Attendant

Clinical Tutor – Histopathology

Senior Manager, Global Device Quality

Associate Manager, Environmental Health and Safety

Director, Combination Product Development

Project Management Officer - Lead

Director Regulatory CMC Sciences Project Management

CSV Engineer (FTC 12 Months)

Materials Engineer – Bitumen & Surface Treatments

Program Manager, Device Technical Operations ( 12 Months Agency Contract )

Cardiac Physiologist Senior

Staff Nurse - Endoscopy

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