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Regulatory Affairs Consultancy Manager Market Authorisations

South East England

£35000 - £45000 per annum

Permanent

NonStop Pharma are currently partnered with a small, growing pharmaceutical consultancy to find a Regulatory Affairs Manager to expand the team.

As a result of an exciting strategic vision of growth, this expanding Pharma company are developing a Regulatory Affairs division. This will join forces with their already established QA & GMP consultancy teams to create a highly effective, exciting portfolio of services to offer their range of clients.

Subsequently, the CEO is looking for a strong, organised and driven individual to manage the Regulatory Services.

The client base is heavily Generics focused, with particular emphasis needed on Market Authorisations & Post Marketing Submissions. Although the clients have a heavy EU emphasis, the company has successful clients overseas, so Chinese and Asian market knowledge can also be utilised, although this is by no means essential.

The successful applicant will be independently leading and starting their own division, with already established clients to be networked with. You will therefore be involved in senior manager meetings surrounding strategy & implementation. They may be a small Business Development element, also.

Ultimately, the client requires someone who has several years of EU experience and can provide expert MA and PostMarketing Regulatory knowledge, particularly in Europe.

This position will suit an ambitious, driven Regulatory Affairs professional, who is excited by the prospect of building excellent client relationships, and building their own consultancy team as a part of rapid company growth.

The successful candidate will benefit from a rare opportunity to build their own team and career very quickly, with no restrictions on their own growth and enjoying an already established and untapped client base.

Benefits:

Work in relatively new, growing Pharma company; be a senior figure by joining at right time

Hire, grow and lead your own team of successful Regulatory consultants

Work closely with senior CEO and company heads; gain great exposure

Be a part of strategy and systematic company planning

Implement your own consultancy plan and lead on client projects

Gain incredible career development opportunities by joining at the right time; be part of company growth

Work with a range of generics products and clients

Provide excellent strategic insight and help improve patient welfare by getting products to market

Be an expert on a variety of postmarketing submissions, including MAAs

Due to companys global outreach, work in variety of markets, including Asian markets

Position Requirements

5 10 years of Regulatory Affairs experience

Extensive experience with a range of generics products

Extensive experience with postmarketing submissions

In depth experience and knowledge with MAAs (Market Access Authorisations)

Strong knowledge of EU Regulatory Affairs

Investigational products experience beneficial e.g. INDs

Experience with Chinese and Asian market Regulatory submissions beneficial

For a confidential discussion about this, please contact Edward Little on (EXT: 7168) or send your updated CV in a word document to #########

NonStop NonStopis one of the largest and fastest growing specialised life sciences recruitment companies in Europe. We are proud members of the APSCo APSColife sciences group who ensure we meet the highest quality standards within the recruitment industry. Our offices are located in the UK, Switzerland and the Czech Republic and we hold labour leasing licences across Europe. Please visit our website for a full list of the niche markets we cover.

Posted 21 days ago

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