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Senior pharmaceutical regulatory specialist

Nenagh
beBeeRegulatory
Biostatistician
Posted: 12 July
Offer description

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.

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