At a Glance
- Tasks: Lead regulatory strategy and manage submissions for innovative therapies in Europe.
- Company: Join a forward-thinking pharmaceutical company dedicated to improving patients' lives.
- Benefits: Competitive salary, inclusive culture, and opportunities for professional growth.
- Other info: Dynamic team environment with a commitment to diversity and inclusion.
- Why this job: Make a real impact on healthcare by guiding cutting-edge products to market.
- Qualifications: Degree in Pharmacy or Life Sciences with strong EMA regulatory experience.
The predicted salary is between 51750 - 63250 £ per year.
We are supporting a pharmaceutical company committed to delivering innovative therapies that improve patients’ lives in recruiting a Senior Regulatory Manager. Their global teams collaborate to bring cutting-edge solutions from concept to market while maintaining the highest standards of quality and compliance.
The Role:
We are seeking an experienced Senior Regulatory Manager with strong expertise in EMA regulatory affairs to join their dynamic team. This role offers the opportunity to lead regulatory strategy, manage submissions, and act as a key regulatory advisor for our product portfolio across the European region.
Key Responsibilities:
- Develop and execute regulatory strategies for products under development and marketed products in Europe, ensuring alignment with EMA requirements.
- Lead and manage EMA submissions, including MAA, variations, line extensions, and renewals.
- Act as primary liaison with EMA, competent authorities, and other regulatory bodies.
- Provide regulatory guidance to cross-functional teams (R&D, clinical, quality, commercial) throughout the product lifecycle.
- Evaluate and interpret new regulations, guidance, and industry trends to ensure ongoing compliance.
- Contribute to internal audits, inspections, and regulatory intelligence initiatives.
Qualifications & Experience:
- Bachelor’s or Master’s degree in Pharmacy, Life Sciences, or related discipline.
- Strong regulatory affairs experience with a focus on EMA submissions.
- Proven experience in preparing and submitting MAA, CTD dossiers, variations, and renewals.
- Strong understanding of EU pharmaceutical regulations and guidelines.
- Excellent written and verbal communication skills.
- Demonstrated ability to lead projects and influence cross-functional teams.
Park Street People Ltd is an Equal Opportunities Employer. We do not discriminate on the grounds of age, race, gender, disability, creed or sexual orientation and comply with all relevant UK legislation. We are acting as an Employment Business in relation to this role.
Senior Manager, Contracts Management in London employer: Park Street People
Join a leading global pharmaceutical company in Chester, where innovation meets a supportive work culture. As a Corporate Benefits Specialist, you'll enjoy competitive remuneration, comprehensive benefits, and ample opportunities for professional growth in a dynamic environment that values diversity and inclusion.
