Pharmiweb.com RSS Feed Pharmiweb.com RSS Feeds

Pharmiweb.com RSS Feed PharmiWeb Candidate Blog

Pharmiweb.com RSS Feed PharmiWeb Client Blog

Job Details

Regulatory Affairs Associate Director – Brussels - Lead global regulatory submissions with Health authorities for a small but expanding Biotech Co.

Company: Advanced Regulatory (EU Roles)
Location:
Reference: TMADV / RA Associate Director – Brussels
Closing Date: 16 Aug 14
Type: Full Time
Salary (£): On Application
Benefits: On Application

Job Summary:

Join a small but expanding biotech company in role where you will take a leading position submitting global regulatory strategies for a number of recently approved products. Contact Theo Moore on +44 207 801 3384 or send a CV in confidence to CV@advregulatory.com

Requirements:

Regulatory Affairs Associate Director – Brussels- Lead global regulatory submissions with the Health authorities for small but expanding Biotech

Location: Belgium, Brussels

Salary up top 100,000 Euros + Car + Bonus + Re-location Package + Pension

Operating as the Regulatory Affairs Associate Director for a small but expanding biotech company you will take a leading position submitting global regulatory strategies for a number of recently approved products. This is an exciting time and you will experience significant visibility, the opportunity to influence and true recognition for your efforts.

Your role will be to prepare or co-ordinate the preparation of Regulatory dossiers (e.g. clinical trials applications, marketing authorisation applications, variations, marketing authorisation renewals etc.) in a timely and efficient manner in accordance with current Regulatory requirements and to authorise their submission in line with defined procedures.

You will manage the Regulatory process to ensure timely approvals of commercially successful products and sit on designated project teams and to provide Regulatory input to these teams. You will also propose Regulatory Strategies and ensure that projects have a current Regulatory Strategy and submission plan.

Required Experience:
Ideally you will have Chemistry, pharmacy or life science degree, PhD potential with 8-12 years’ experience in Regulatory Affairs. Good knowledge of European Regulatory procedures and requirements; Technical Regulatory experience of biological biotechnological products preferred.

 

If you wish to apply for this role please click below, or send your CV with a covering note to cv@advregulatory.com quoting reference number noted above. Alternatively to have a confidential discussion about this or other potential roles or career options call Theo Moore or  Matt Greig in the UK London office, on +44 (0)207 801 3380.
_______________________________________________________________________________________

About Advanced

Advanced Regulatory is a division of Advanced Search and Selection Ltd and have been operating since 2004. We are registered and licensed to recruit in the UK, Belgium & Switzerland - we have an office both in the UK and Switzerland. We are a recruitment business dedicated to the pharmaceutical industry, specialising in Regulatory Affairs. We match professional candidates to the best permanent, contract and interim roles in the market. For more information about the company visit us at www.advregulatory.com or to have a confidential discussion about this role, or any other roles, please contact Theo Moore or Matt Greig on +44(0)207 801 3380.

We provide a high level of service because we believe this matters. Regulatory professionals will find we know our recruitment subject matter.

Keywords / Key words: Regulatory, Regulatory Affairs, Reg Affairs, RA, Regulatory jobs, RA jobs, Regulatory Affairs Jobs.

To Apply : Please send a full CV in confidence to cv@advregulatory.com.

Contact Information:

Address:  Head Office
1 Calico House
Clove Hitch Quay
Plantation Wharf
Battersea
London
SW11 3TN
England
Tel:  +44 (0)207 801 3380
Website:  Visit Our Web Site

Advertising