Find Policy Jobs in Dublin, D

Manager, EU & International Regulatory Affairs, Global Rare Diseases
Chiesi Farmaceutici —Dublin, County Dublin
- Research
- Leadership
- Communication skills
Payments & Compliance Co-Ordinator (Financial Operations)
Trinity College Dublin —Dublin, County Dublin
- €47,848–€59,847 a year
- Full-time
9d
Head of Risk, Compliance and Assurance (AP Grade)
Irish Medical Council —Dublin, County Dublin
- €83,113 a year
- Full-time
- Hybrid work
- Continuous improvement
- Business
- Leadership
- Annual leave
- Employee assistance program
Quick apply
Head of Risk & Compliance
Evelyn Partners —Dublin, County Dublin
- €175,000–€185,000 a year
- Full-time
- Hybrid work
- Presentation skills
Quick apply
9d
Public Affairs Manager
Eirgrid —Dublin, County Dublin
- Full-time
- Research
- Analysis skills
- Project management
Quick apply
6d
Healthcare Quality & Compliance Officer (CORU/NMBI)
Comfort Keepers Ireland —Dublin, County Dublin
- Full-time
- Nursing
- Microsoft Access
- Microsoft Office
- Fuel card
11d
Manager, Regulatory Affairs
Azurity Pharmaceuticals - Ireland —Dublin, County Dublin
- English
- Bachelor's degree
- Communication skills
Compliance, Regional Country Compliance, Vice President, Dublin
Goldman Sachs —Dublin, County Dublin
- Full-time
- Analysis skills
- Bachelor's degree
- In-person
- Employee assistance program
Head of Legal for Research & Innovation
Trinity College Dublin —Dublin, County Dublin
- €111,114–€148,547 a year
- Full-time
Country Compliance & Operational Risk Manager
Bank of America —Dublin, County Dublin
- Full-time
- Bachelor's degree
- No degree
- Business
- Employee assistance program
Head of Global Regulatory Strategy, Global Regulatory Affairs
Viatris —Northern Cross, County Dublin
- Full-time
- Doctoral degree
- Master's degree
- Business
Patient Care Compliance Agent
Air Liquide —Dublin, County Dublin
- Full-time
- Customer service
- Bachelor's degree
Head of Information Security, Risk & Compliance
Glanbia Foods —DUBLIN 24, County Dublin
- Master's degree
- Bachelor's degree
- No degree
Research Scientist: Machine Learning for Drug Discovery and Genomic Data
Accenture —Dublin, County Dublin
- Full-time
- Doctoral degree
- Computer Science
- English
Head of Compliance and Chief Risk Officer
Marsh Finance —Dublin, County Dublin
- Full-time
- No degree
- Business
- Leadership
Quick apply
Research Engineer: Machine Learning and Knowledge Representation for Biodata
Accenture —Dublin, County Dublin
- Full-time
- Computer Science
- English
- Research
Head of Compliance
Macquarie Group Limited —Dublin, County Dublin
- Full-time
- Leadership
- Communication skills
Head of Compliance and Money Laundering Reporting Officer
Aon Corporation —Dublin, County Dublin
- Full-time
- Analysis skills
Building Safety and Compliance Officer
Tuath Housing Association —Dublin, County Dublin
- Full-time
Quick apply
Associate Director, CMC Regulatory Affairs (Hematology/Oncology)
Regeneron —Dublin, County Dublin
- €101,500–€165,200 a year
- Bachelor's degree
- No degree
- In-person
- Annual leave

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Manager, EU & International Regulatory Affairs, Global Rare Diseases

Chiesi Farmaceutici -
Dublin, County Dublin

Apply Now

Job details

Permanent

Qualifications

Research
Leadership
Communication skills
Time management

Full job description

Date: 11 Jul 2026

Department: GRD Regulatory Affairs

Business Area: R&D, Pharmacovigilance & Regulatory Affairs

Job Type: Direct Employee

Contract Type: Permanent

Location:

Dublin, IE

About us

Chiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in Parma, Italy. More than 8,000 employees across the group are united by a singular purpose: promoting a healthier world for our people, patients, and the planet. This is what drives us as we research, develop, and market innovative drugs across our main therapeutic areas. Discover more here.

At Chiesi we are thinking generations ahead, driving sustainable innovation with purpose. This fosters a culture of reliability, transparency, and ethical behaviour at every level. As a Benefit Corporation and a certified B Corp, we have embedded sustainability in our bylaws and continuously measure our impact.

Diversity and inclusion are at the heart of who we are. We believe our differences make us stronger. We are a vibrant ecosystem of passionate, talented individuals united by strong values, each bringing unique perspectives that help us to continuously challenge the status quo for the better.

Chiesi Global Rare Diseases

Chiesi Global Rare Diseases is a Chiesi Group’s business unit established in February 2020 and focused on research, development and commercialization of treatments and patient support services for rare and ultra-rare disorders, many of whom have limited or no treatments available.

This unit is based in Boston, Massachusetts, with a strong synergy with the headquarters in Parma.

Rare unit has a focus on research and product development for lysosomal storage diseases, rare hematology, ophthalmology disorders and rare immunodeficiencies. The unit is also a dedicated partner with global leaders in scientific research, patient advocacy and care. Discover more here.

What we are looking for

This is what you will do

Reporting to the Lead, EU & Int'l Regulatory Affairs, Global Rare Diseases, the Manager, EU & International Regulatory Affairs develop regulatory strategies for EU & International markets to meet Chiesi Global Rare Diseases Regulatory Affairs relevant objectives.

You will be responsible for

In collaboration with consultants, partners and affiliates, plan, coordinate and manage regulatory submissions to regional agencies throughout the life cycle of GRD products
In full alignment with the Lead, EU & Int'l Regulatory Affairs, Global Rare Diseases, provide advice and guidance regarding regional regulatory requirements driving the development and geographical expansion of GRD products.
Contribute to the preparation and/or review of submissions to relevant markets to ensure the high quality of the documentation
In agreement with the Lead, EU & Int'l Regulatory Affairs, Global Rare Diseases, communicate directly with regional regulatory authorities on behalf of Chiesi GRD to negotiate strategies and actions associated with regulatory submissions
Critically review regulatory submission documents, periodic updates, overviews, summaries, etc., make recommendations for improvement and ensure adequacy for submission.
Contributes to the development of processes and the preparation of Standard Operating Documents for GRD Regulatory Affairs
In full alignment with the Lead, EU & Int'l Regulatory Affairs, Global Rare Diseases, provide regulatory guidance to colleagues from other functional areas
Provide regulatory expertise in support of due diligence assessments
Represent the Regulatory Department at the Core Team as a global RA member, where needed
Support the Lead, EU & Int'l Regulatory Affairs, Global Rare Diseases in the preparation of the needed documents for the meetings and interactions with regional regulatory authorities

You will need to have

3 to 5 years of experience in corporate regulatory affairs roles with an in-depth knowledge in the drug development
Life Science Degrees
Flexible, collaborative, open minded
Well-developed written and oral communication and listening skills
Time management skills and demonstrated ability to manage complex assignments
Well-developed analytical and problem-solving skills
Ability to work independently and as part of a team

We would prefer for you to have

Experience in leadership and coaching is an asset

What we offer

No matter where your path starts at Chiesi, it leads to inspiring possibilities. Your future is our focus, and we are committed to nurturing your development in our dynamic, friendly environment with access to resources and training every step of the way.

We provide top-class benefits, including comprehensive healthcare programs, work-life balance initiatives, and robust relocation support. Our salary package is competitive, comprising a basic salary, performance bonuses, and benefits benchmarked against the external market. Additionally, we offer flexible working arrangements, remote work options, and tax assistance services for foreign colleagues, all designed to help you thrive.

Chiesi is an equal opportunity employer committed to hiring a diverse workforce at all levels of our business. All qualified applicants receive consideration for employment based on attitude and merit, without regard to race, national origin, age, sex, religion, disability, sexual orientation, marital status, military status, gender identity or expression, or any other basis protected by applicable laws. This policy applies to all aspects of employment, including hiring, transfer, promotion, compensation, eligibility for benefits, and termination.

Apply Now

Refine Your Search

policy jobs in dublin, d

Manager, EU & International Regulatory Affairs, Global Rare Diseases

Payments & Compliance Co-Ordinator (Financial Operations)

Head of Risk, Compliance and Assurance (AP Grade)

Head of Risk & Compliance

Public Affairs Manager

Healthcare Quality & Compliance Officer (CORU/NMBI)

Manager, Regulatory Affairs

Compliance, Regional Country Compliance, Vice President, Dublin

Head of Legal for Research & Innovation

Country Compliance & Operational Risk Manager

Head of Global Regulatory Strategy, Global Regulatory Affairs

Patient Care Compliance Agent

Head of Information Security, Risk & Compliance

Research Scientist: Machine Learning for Drug Discovery and Genomic Data

Head of Compliance and Chief Risk Officer

Research Engineer: Machine Learning and Knowledge Representation for Biodata

Head of Compliance

Head of Compliance and Money Laundering Reporting Officer

Building Safety and Compliance Officer

Associate Director, CMC Regulatory Affairs (Hematology/Oncology)

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