Senior Director Regulatory Affairs
- Employer
- MSI Pharma
- Location
- England
- Salary
- Negotiable
- Start date
- 5 Aug 2024
- Closing date
- 12 Aug 2024
View more
- Discipline
- Regulatory Affairs
- Hours
- Full Time
- Contract Type
- Permanent
- Experience Level
- Senior Management
Job Details
We are seeking a dynamic and experienced professional to join our client's team as the Senior Director of Regulatory Affairs for the Northern European Cluster. You will based in the South-East of England, working in a hybrid work environment. In this role, you will be at the forefront of regulatory strategy, guiding product registrations, line extensions and new indications to align with our client's business objectives. Your expertise will ensure compliance with relevant regulations and quality system requirements, driving operational excellence and strategic vision.
Key Responsibilities:
- Leadership & Management: Oversee the Northern Europe Cluster personal Healthcare products Regulatory Affairs team, managing the regulatory budget and fostering a culture of operational excellence.
- Strategic Vision: Develop and implement product positioning strategies, providing critical regulatory insights to R&D and clinical leads.
- Regulatory Expertise: Navigate and interpret regulatory landscapes to inform product positioning, competition, and risk management.
- External Relationships: Represent a world-leading consumer health company with regulatory agencies and industry associations, maintaining and cultivating essential external relationships.
- Regulatory Strategy: Lead the evaluation of risk and safety issues, recommend regulatory solutions, and oversee regulatory strategies to ensure compliance and protect corporate interests.
- Compliance Oversight: Approve regulatory filing strategies, manage regulatory interactions, and adapt strategies based on legislative changes.
- Advocacy & Innovation: Stay abreast of scientific and clinical advances, drive new regulatory approaches, and engage with stakeholders to shape science-based regulatory decision-making.
Qualifications:
- Bachelor's degree or higher in a relevant field.
- 10+ years of related Regulatory Affairs experience.
- Strong proven Leadership experience across global teams
- Expertise across a broad spectrum of Regulatory classifications, including Medicinal products, Cosmetics, Commodities, and/or Medical devices.
- Consumer health or OTC (over-the-counter) previous experience would be highly desirable
- Solid understanding of Regulatory, medical, Safety, and Quality requirements.
- Proficiency in English.
The client will consider candidates from outside the UK who are willing to relocate, if you have the gravitas and leadership qualities to succeed in a Senior Director level Regulatory Affairs role.
Why Join our client?
As a world-leading consumer health company, our client believes in creating a positive impact on health-care through innovative regulatory strategies and compliance excellence. As the Senior Director of Regulatory Affairs, you will have the opportunity to lead a talented team, influence key regulatory decisions, and shape the future of our products in the Northern European market. If you are a visionary leader with a passion for Regulatory affairs and a commitment to excellence, this could be the ideal role.
Please Send your latest resume and a cover letter outlining your experience and vision for the role or call me on 02079401985 if you require further information
Company
Founded in 2011, MSI Pharma specialises in recruitment and talent acquisition for pharmaceutical, biotech and life sciences staff on a permanent and interim basis.
We work in partnership with leading global brands and have a presence in the UK, DACH region, and North America.
- Website
- https://www.msigroupltd.com/
- Location
-
2nd Floor, Goat Yard
Albion House
20 Queen Elizabeth Street
London
SE1 2RJ
United Kingdom
Get job alerts
Create a job alert and receive personalised job recommendations straight to your inbox.
Create alert