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Director Regulatory Affairs: Vaccines, Biologics; development

Employer
NonStop Consulting
Location
Brussels
Salary
car + package
Closing date
Mar 19, 2021

View more

Sector
Science, Life Sciences, Anatomy/Physiology
Contract Type
Employee
Hours
Full Time
Organization Type
Corporate

Job Details

My client, a large pharmaceutical company, is looking for their next Director of Regulatory Affairs to head their Vaccines & Biologics division.

As a part of the regulatory team, your role as director will be to properly coordinate all regulatory projects and make sure the RA division is running like a well-oiled machine.

Responsibilities include but are not limited to:


- Manage people in your team and for the assigned projects;

- Develop EU product regulatory strategy and optimise label, obtain shortest time to approval by regulatory agencies

- Develop product regulatory strategy for non-EU countries in the RAE region (CH and non-EU CES)

- Oversee the maintenance of all vaccines & biologicals in your assigned therapeutic area and be responsible for regulatory compliance of these products in the EU region;

- Responsible for all RA procedures in the region for the assigned projects and therapeutic area, including PIP applications, local and regional Scientific Advice, MRP, DCP, CP and national procedures

- Conduct due diligence licensing candidate review;

- Responsible for regulatory review and final approval of all submissions and associated documentation for the assigned vaccines/ biologicals;

- Provide support to the RA subsidiary team on subjects related to the projects or therapeutic area

- Provide EU expertise to the worldwide RA team, the product development teams and the Vaccines franchise;

- Be a recognised, internal expert (SME) for one or more aspects of regulatory policy and recognised as a scientific expert in one or more therapeutic areas.

Your ideal profile:

- Formal scientific background (Master's degree minimum in pharmaceutical sciences, biochemistry, etc...)

- At least 8-10 years of experience in Regulatory Affairs on Development level. Life Cycle Management experience strongly appreciated

- Previous experience with Vaccines/Biologics is required; experience with Infectious Diseases is a big plus

- Strong people management skills

- Strong negotiation skills (for contact with relevant authorities)

Company

Our Consultants are trained to deliver an exceptional standard of recruitment services to clients across the life sciences, chemical, care, educations, technical, digital and finance industries. 

Our clients – and bottom line profits - tell us that we do a great many things very well. Complacency, however, is the last word you would associate with us. We work incredibly hard to deliver better and better results, based on stronger and stronger service delivery.  Which is why we believe the best is yet to come – for us, our clients and for the people who have what it takes to join us on the journey.

The result? We’re expanding (in the UK and across Europe and even to Boston, US) and continue to post impressive performances in all our niche sectors. 

Company info
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