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Regulatory Affairs Manager
4 weeks ago
Group Regulatory Affairs Manager – Pharmaceuticals (Hybrid)
Location: Offices based near Dunboyne, Co. Meath, Ireland
Our client is a thriving Irish pharmaceutical group experiencing significant growth. Through consistent organic expansion and strategic acquisitions they have built a strong portfolio of market-leading OTC and Prescription medicines. Their products are marketed across numerous EU countries, Australia, and New Zealand.
Due to their continued expansion, they are seeking a highly motivated and experienced Group Regulatory Affairs Manager to join their growing team. This is a fantastic opportunity to make a tangible impact within a dynamic, family-run business that prioritises performance and offers excellent career progression.
What You'll Do:
As the Group Regulatory Affairs Manager, you'll play a crucial role in ensuring the clients diverse product portfolio complies with global regulatory frameworks. This is a hands-on management position where you'll be expected to get stuck in and drive results. Your key responsibilities will include:
- Developing and implementing robust regulatory strategies to support product development and lifecycle management, particularly for our expanding portfolio acquired through acquisitions.
- Leading and mentoring a team of Regulatory Affairs Officers, fostering a collaborative and high-performing environment.
- Efficiently integrating all new portfolio acquisitions across multiple international markets.
- Spearheading projects to identify and resolve gaps in regulatory dossiers.
- Leading high-level meetings with Regulatory Authorities.
- Driving the regulatory aspects of internationalizing products and pursuing reclassification when appropriate.
- Proactively monitoring and interpreting global regulatory trends and changes, ensuring the company is always ahead of the curve.
- Collaborating cross-functionally with our Quality and Commercial/Marketing teams to achieve overarching company objectives.
What You'll Bring:
Our client is looking for a resilient and adaptable individual with a strong sense of ownership and a proven track record in regulatory affairs.
Essential Experience & Knowledge:
- 8-10 years of progressive experience in Regulatory Affairs within the pharmaceutical industry (human health).
- Strong knowledge of global regulatory frameworks, including MRP, DCP, and CP procedures.
- Demonstrable experience with pharmaceutical products, specifically OTC and/or prescription medicines, with a focus on preparing and submitting dossiers for multiple EU countries.
- A proactive, "roll up your sleeves" attitude with a strong drive to see tasks through to conclusion.
- Exceptional attention to detail and outstanding organisational skills.
- Ability to work autonomously, take initiative, and assume responsibility for your actions.
Highly Desirable:
- Knowledge of medical device regulations.
- Experience with cosmetics regulations.
What's On Offer:
- Competitive Salary: A highly competitive salary, negotiable based on your experience. For a manager-level role like this.
- Performance-Based Bonuses: Your hard work and contributions will be recognized and rewarded through performance-based bonuses.
- Hybrid Working: Our client embraces a hybrid working model to offer flexibility while fostering team collaboration. You'll be required in their offices near Dunboyne, Co. Meath three days a week. They offerflexible start and finish times around their contracted 9-5 hours to help avoid peak traffic.
- Career Progression: With a turnover of €250 million and ambitious growth plans, the opportunities for professional development and career advancement within the company are significant.
If you're a seasoned Regulatory Affairs professional looking for a challenging yet rewarding role within a rapidly expanding pharmaceutical group, we encourage you to apply
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