Description
This client is one of the fastest growing pharmaceutical companies in UK, and is rapidly expanding into Europe.As the Regulatory Affairs Manager, you shall combine your knowledge of scientific, legal and business issues to ensure products, which are developed, manufactured or distributed by a wide range of companies, meet the required legislation.
Key Responsibilities:
* Ensuring product compliance with the regulations of MHRA and EU authorities
* Keeping abreast of international legislation, guidelines and customer practices in all countries that the company is exporting to
* Preparing submissions of license variations and renewals to strict deadlines
* Ensure the appropriate licensing, marketing and legal compliance of pharmaceutical and medical products in order to control the safety and efficacy of products
* Manage and mentor direct reports
* Fluency in written/spoken English is essential
* Must be eligible to work in UK
The ideal candidate will hold a relevant life science or chemistry degree; have a minimum of 4 year's regulatory affairs experience in the pharmaceutical industry. You should be a motivated, driven, confident and influential individual with excellent problem solving, communications and computer skills.
For further information, please contact Karan Baxi on or via email on ka.baxi(a)realstaffing.com who specialises in placing regulatory professionals in varying levels of seniority.
Additionally, the wider Regulatory team have a range of roles that they are currently recruiting for so if you are looking for something other than this role, please do get in touch on .
To find out more about Real please visit www.realstaffing.com