Regulatory Affairs Specialist
Location: Dublin
Type: Permanent
Salary: €55,000 – €75,000 DOE
About the Role
Our client, a growing pharmaceutical and medical device organisation based in Dublin, is seeking a Regulatory Affairs Specialist to join their quality and compliance function. The successful candidate will play a key role in managing regulatory submissions, maintaining product compliance, and supporting new product introductions.
Key Responsibilities
- Prepare and submit regulatory documentation for new and existing products (IMB/EMA/FDA).
- Maintain regulatory approvals and ensure compliance with applicable legislation.
- Support product registration, variations, and renewals globally.
- Liaise with internal teams to provide regulatory guidance during product development.
- Monitor evolving regulations and assess their impact on company products.
Skills & Experience
- Degree in Science, Pharmacy, or a related field.
- Minimum 3 years’ experience in Regulatory Affairs within pharma, biopharma, or medtech.
- Strong knowledge of EU and FDA regulatory requirements.
- Excellent written and verbal communication skills.
- Ability to work effectively across cross-functional teams.
What’s on Offer
- Opportunity to influence compliance and innovation in a growing Life Science company.
- Competitive salary and flexible working arrangements.
- Career progression within an expanding international environment.
Why Choose Clark
Clark Recruitment is a trusted recruitment partner to the Life Sciences industry in Ireland. Based in Naas, Co. Kildare, and operating since 1998, we combine deep local knowledge with national reach. Our consultants take time to understand your ambitions and connect you with employers where your skills and career can thrive.
INDCLA
Clark Recruitment Ltd. is an equal opportunities employer. We are committed to fostering a diverse and inclusive workplace. All applications are treated in the strictest confidence, and we welcome candidates from all backgrounds to apply.