Job Details

Job Summary:

Join a leading Ethical Pharmaceutical company in a role that comes with EU CP & DCP MAA project responsibility. Receive a great salary and excellent training in a friendly, motivated regulatory team that is highly respected within the organisation. Contact Theo Moore on +44 (0)207 801 3384 or email me on Cv@advregulatory.com to apply.

Requirements:

Regulatory Affairs Snr Manager – Berks/Bucks Borders - Join an expanding Global Pharmaceutical co where you can grow, develop and lead EU submissions

Location: Berks/Bucks Borders, commutable from London, the M4 corridor, Oxford, Herts and Hampshire

We have a number of new and exciting regulatory affairs roles for a successful leading Global Pharmaceutical company based in Berks/Bucks Borders who are looking for a number of forward thinking regulatory affairs professionals who would like to lead Regulatory projects for EU submissions for both pharma and biotech projects.

This is a great time to join an organisation that likes to give regulatory professionals challenging projects and clear and defined career development opportunities. You will be joining a friendly, motivated regulatory team that is highly respected within the organisation.

In the short term you will lead and manage Regulatory submissions for Pharmaceutical projects via the CP & DCP, whilst in the long term you will be given the opportunity to become the company specialist in certain aspects of regulatory affairs.

The therapeutic areas and dosage formulations are varied and cover small molecules and Biologicals. This is a real learning company, one where you will have a succession plan and real career development.

Role:
• Responsible for the preparation and submission and regulatory approval of new marketing authorisation applications within Europe as required
• Responsible for the maintenance of existing marketing authorisations as required
• Communications with the EMEA to expedite new marketing authorisation approvals and maintenance of marketing authorisations

The salaries for these roles are up to £70,000 plus Car + Bonus and come with an excellent benefits - You will need 8-12 years in European regulatory affairs, combined with a proactive approach and ability to work in a matrix with good problem-solving skills.

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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, French and German speaking candidates should call Marc Van de Voorde in our Swiss office, on +41 (0)78 170 4042 and for candidates from the UK, NL and rest of world call Matt Greig or Theo Moore, in the UK London office, on +44 (0)207 801 3380.
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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.