Find manager, regulatory affairs Jobs in dublin, d

Manager, Regulatory Affairs
Azurity Pharmaceuticals - Ireland —Dublin, County Dublin
- English
- Bachelor's degree
- Communication skills
Manager, Regulatory Affairs
Azurity Pharmaceuticals - US —Dublin, County Dublin
- English
- Bachelor's degree
- Communication skills
Manager Corporate Drug Regulatory Affairs (12 month agency contract)
Viatris —Northern Cross, County Dublin
- Full-time
- English
- Bachelor's degree
- Communication skills
Traveller Liaison & Traveller Accommodation Programme Manager
Fingal County Council —Fingal, County Dublin
- €61,217–€79,583 a year
1d
Director, Regulatory Affairs Medical Devices & Combination Product
Takeda Pharmaceutical —Dublin, County Dublin
- €116,800–€160,600 a year
- Full-time
- English
- Bachelor's degree
- Communication skills
10d
Pharma Partnerships Manager
Optum —Dublin, County Dublin
- Full-time
- Negotiation
Senior Manager, Regulatory Affairs CMC
Viatris —Northern Cross, County Dublin
- Full-time
- Microsoft Office
- Project management
Assistant Manager, Regulatory Affairs CMC (Global)
Viatris —Northern Cross, County Dublin
- Full-time
- Microsoft Office
- Manufacturing
Chief Technology Officer
FOODHUB —Dublin, County Dublin
- €200,000–€400,000 a year
- Full-time
- Hospitality
- Computer Science
- In-person
- Annual leave
Quick apply
3d
Compliance Manager
ESB —Dublin, County Dublin
- €86,300–€101,600 a year
- Full-time
- Organisational skills
- SharePoint
- Communication skills
8d
Ireland Partnerships Lead - Inclusive Design
See Me Please Ltd —Dublin, County Dublin
- €52,813.79–€180,000.00 a year
- Full-time
- Sick pay
Quick apply
12d
Manager, People Business Partnerships, EMEA & APAC
Clio —Dublin, County Dublin
- €96,800–€145,200 a year
- Full-time
- English
- Master's degree
- Bachelor's degree
Sr Dir CMC Regulatory Affairs
Regeneron —Dublin, County Dublin
- Bachelor's degree
- In-person
- Leadership
- Annual leave
Head of Global Regulatory Affairs Strategy
Viatris —Northern Cross, County Dublin
- Full-time
- Doctoral degree
- Master's degree
- Business
10d
Senior Manager, Global Regulatory Affairs – Business Process
Viatris —Northern Cross, County Dublin
- Full-time
- Project management
- No degree
Senior Manager, European Regulatory Policy and Intelligence
Viatris —Northern Cross, County Dublin
- Full-time
- Communication skills
- Marketing
10d
Sr. Internal Communications Director
Glanbia Foods —DUBLIN 24, County Dublin
- €170,000–€215,000 a year
- Hybrid work
- Business
Senior Manager Regulatory Intelligence
Regeneron —Dublin, County Dublin
- Analysis skills
- Organisational skills
- In-person
- Annual leave
Implementation Manager
Front —Dublin, County Dublin
- €85,000–€96,800 a year
- Full-time
- Hybrid work
- English
- Project management
- Communication skills
- Annual leave
Data Manager
dnata Catering Ireland Limited —Saint Margaret's, County Dublin
- €75,000–€80,000 a year
- Full-time
- Microsoft Excel
- SQL
- Analysis skills
- Sick pay
Quick apply

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Manager, Regulatory Affairs

Azurity Pharmaceuticals - Ireland
Dublin, County Dublin

Apply Now

Job details

Qualifications

Biology
English
Bachelor's degree
Communication skills
Marketing

Full job description

Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. As an industry leader in providing unique, accessible, and high-quality medications, Azurity leverages its integrated capabilities and vast partner network to continually expand its broad commercial product portfolio and robust late-stage pipeline. The company's patient-centric products span the cardiovascular, neurology, endocrinology, gastro-intestinal, institutional, and orphan markets, and have benefited millions of patients. For more information, visit www.azurity.com.

Azurity Pharmaceuticals is proud to be an inclusive workplace and an Equal Opportunity Employer. Azurity's success is attributable to our incredibly talented, dedicated team that focuses on benefiting the lives of patients by bringing the best science and commitment to quality into everything that we do. We seek highly motivated individuals with the dedication, integrity, and creative spirit needed to thrive in our organization.

Brief team/department description:

Manager, Regulatory Affairs: Managing EU and International Regulatory activities for assigned projects

Manage the regulatory filings of medicinal products via EU centralized procedure as well as MRP/DCP/NP procedures, including but not limited to MAAs, variations, MATs, and other associated life cycle maintenances submissions. Main role is to be a primary interface with the EMA and maintaining good working relationship with Product Leads, Rapporteurs, CHMP members and other EMA officials to secure timely approval of filings. Support in International territories in Life cycle maintenance.

Principle Responsibilities:

Manage and coordinate regulatory submissions for all projects to include but not limited to Scientific Advice, Pediatric Implementation Plan submissions, MAAs, variations and other associated life cycle maintenances submissions.
Develop and implement regulatory strategies for product registration and life cycle
Lead cross-functional discussions to align on submission strategies, prioritize activities, and establish realistic implementation timelines for regulatory activities based on the cross-functional requirements.
Review labelling (SPC, PIL and Labelling) to ensure compliance against current guidelines and standards
Review change controls for the regulatory team
Ownership of all outside communication with EU/EEA Health Authorities (EMA, National
Competent Authorities) on behalf of the Company
Provide guidance to support with regulatory related questions and complaints
Monitor evolving regulatory requirements and provide proactive advice to cross functional teams
Follow company policies and procedures
Contribute to generate and review SOPs and Work instructions
Periodically reviewing the product information (SPC, PIL and Labelling) for compliance against the Core Safety Information (CSI) as well as current EU guidelines and standards
Manage the artwork preparation and approval process of printed packaging components to meet packaging design and legislation requirements for each new product, new packs, or changes to existing packaging
Managing publishing and translation activities with support from partner CRO
Support review of EU promotional material

Qualifications and Education Requirements

Bachelor of Science, Biological Sciences or other related area of study
5-7+ years of experience in Regulatory Affairs especially with European, UK exposure
Regulatory Affairs exposure to China would be considered a plus
Proven experience with EMA, NCA's
Strong background in pre-marketing activities and preparation of MAA's
Ability to perform under pressure with limited resources
Excellent communication and presentation skills in English
Strong writing analytical and problem-solving abilities

#LI-Hybrid

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Refine Your Search

manager, regulatory affairs jobs in dublin, d

Manager, Regulatory Affairs

Manager, Regulatory Affairs

Manager Corporate Drug Regulatory Affairs (12 month agency contract)

Traveller Liaison & Traveller Accommodation Programme Manager

Director, Regulatory Affairs Medical Devices & Combination Product

Pharma Partnerships Manager

Senior Manager, Regulatory Affairs CMC

Assistant Manager, Regulatory Affairs CMC (Global)

Chief Technology Officer

Compliance Manager

Ireland Partnerships Lead - Inclusive Design

Manager, People Business Partnerships, EMEA & APAC

Sr Dir CMC Regulatory Affairs

Head of Global Regulatory Affairs Strategy

Senior Manager, Global Regulatory Affairs – Business Process

Senior Manager, European Regulatory Policy and Intelligence

Sr. Internal Communications Director

Senior Manager Regulatory Intelligence

Implementation Manager

Data Manager

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