Regulatory Affairs Manager Job Opportunity
We are seeking an experienced professional to lead regulatory activities, manage submissions, and develop global regulatory strategies for a global pharmaceutical leader.
* Lead regulatory strategy for key projects, ensuring compliance with global requirements.
* Manage regulatory submissions, including new registrations, post-approval changes, renewals, and technical variations.
* Track regulatory commitments, assess risks, and provide strategic input on development plans.
* Act as a scientific and technical resource, mentoring colleagues and sharing expertise.
* Prepare responses to regulatory authority queries, ensuring timely and high-quality submissions.
* Stay updated on evolving regulations and assess their impact on existing and future products.
* Collaborate with internal stakeholders across R&D, Manufacturing, and Regulatory Affairs.
* Engage with regulatory authorities (EU bodies) to support marketing authorisation applications.
* Review GMP documents such as change controls, deviations, and batch manufacturing records.
Requirements
* Experience: Minimum 5+ years in Regulatory Affairs within the pharmaceutical industry.
* Knowledge: Strong understanding of EU and global regulatory frameworks, including HPRA submissions.
* Skills: Excellent project management, communication, and stakeholder engagement.
* Education: Degree in Life Sciences, Pharmacy, or a related discipline.
Benefits
Competitive salary + Annual Incentive Plan.
Work with a global pharma leader in an impactful regulatory role.
Collaborative environment with strong career development opportunities.
Exposure to international markets and regulatory bodies.
This is an exciting opportunity for a regulatory expert looking to take the next step in their career.