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Regulatory Affairs Manager

Central London   •  Negotiable  •  Contract/Temporary, Full time

Regulatory Affairs Manager

Initial 3-6 Month Contract

ASAP start

Remote working

Offering attractive hourly rate DOE

Inside IR35

CPL Life Sciences are collaborating with a leading generic pharmaceutical organisation who have an urgent requirement for a Regulatory Affairs Manager whilst sourcing for a permanent hire. The preferred candidate will have a generics background and have a strong background in Life Cycle Management, supporting MA Approvals.

Job Responsibilities;

- To assist the RA Director to implement the Regulatory Affairs strategy for the EU.

- To undertake regulatory affairs work as required.

- To generate high quality regulatory submissions to target markets throughout Europe in order to deliver a successful and timely portfolio of MA approvals in accordance with the company's requirements.

- Following MA approvals, maintenance of the MA approval activities including preparation and submission of variations and preparation for product launch

Candidate Requirements Include;

- Eligibility to live and work in the United Kingdom

- Relevant experience in pharmaceutical environment, preferably in generics pharma.

- Minimum 5 years experience in Regulatory Affairs

- Experience in working in a multicultural environment.

- Knowledge about submissions requirements in the EU.

If this position is of interest to yourself please forward your up to date CV to sophie.malyon@cpl.com or call on 0118 952 2797.

  • Agency: Cpl Life Sciences
  • Reference: JO-2206-494668
  • Posted: 13th June 2022
  • Expires: 11th July 2022

Cpl Life Sciences

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