Regulatory Affairs Manager job in London, England

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Job type: Contract

Discipline: CMC

Location: United Kingdom

This vacancy has now expired. Please see similar roles below...

Proclinical are recruiting a Regulatory Affairs Manager for a pharmaceutical establishment. This role is on a contract basis and allows for remote working anywhere within the UK. The client is focused on supplying transformative treatments.

Responsibilities:

Guarantee the implementation of international and leadership with the company, as well as guide/partake in the development of new direction, plan, and procedures.
Participate and guide the regulatory CMC mechanisms of corporate-linked projects.
To deliver on the requirements of both the company and the client, you will handle the generation of chemistry, manufacturing and control (CMC) documents for designed product varieties.
You will handle international CMC regulatory proposals guaranteeing that project actions and papers are delivered to the necessary standards across the product lifecycle.
Communicate with shareholders and team members to warrant pertinent timelines and regulatory commitments are transferred.

Skills & Requirements:

Prior involvement with CMC either Biologics or Synthetics.
A clinical background would be advantageous for the role but is not essential.
Present CMC comprehension regarding international proposals, not BAU.
Acquaintance with oncology.

If you are having difficulty in applying or if you have any questions, please contact Peter Duvall at +44 203 0789 542.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

#Regulatory