Global Regulatory Affairs Lead
This is a high-profile role within the pharmaceutical industry, offering an exciting opportunity to lead regulatory activities and develop strategic plans.
* Leverage expertise in EU and global regulatory frameworks to drive submissions and ensure compliance.
* Collaborate with internal stakeholders to advance R&D, manufacturing, and regulatory affairs goals.
* Mentor colleagues and share knowledge on regulatory best practices.
* Represent the organization at industry conferences and advisory committees.
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, stakeholder engagement, and leadership.
Education: Degree in Life Sciences, Pharmacy, or a related discipline.
Advantageous: Experience in CMC, post-market surveillance, and regulatory strategy development.
Benefits:
Competitive remuneration package
Collaborative work environment with strong career development opportunities
Exposure to international markets and regulatory bodies
Professional growth and advancement
We are seeking a highly skilled and experienced individual to fill this challenging position. If you have the necessary expertise and passion for regulatory affairs, apply now.