Regulatory Affairs Consultant

Dependent on experience
10 Jan 2017
07 Feb 2017
Gemma Everitt
Contract Type
Full Time
Hyper Recruitment Solutions are currently looking for a Regulatory Affairs Consultant to join a leading life sciences company based in the Cambridgeshire area. As the Regulatory Affairs Consultant you will be providing regulatory consultancy services to internal and external clients, including preparation, review, submission and project management of regulatory applications.


Your duties as the Regulatory Affairs Consultant will be varied however the key duties and responsibilities are as follows:

1. Prepare, review, submit and project manage regulatory submissions in compliance with the applicable SOPs, regulatory guidelines and legislation.

2. Develop and maintain effective working relationships with internal and external clients, regulatory authorities and suppliers.

3. Maintain electronic and hard copy project and regulatory files.

4. Participate in business development activities as required.


To be successful in your application to this exciting opportunity as the Regulatory Affairs Consultant we are looking to identify the following on your profile and past history:

1. Degree or equivalent qualification in a Science subject.

2. Proven industry experience in regulatory submissions and interactions with the MHRA.

3. A sound technical and scientific understanding of one or more of manufacturing, non-clinical or clinical development of pharmaceutical/healthcare products.

Key Words: Regulatory Affairs, consultancy, submissions, project management, MHRA, manufacturing, clinical, pharmaceutical, healthcare

Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer that is happy to welcome applications for any applicant who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors and is made up of a collaboration of scientists supporting science. We look forward to helping you with your next career moves.

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