This job has expired

Regulatory Affairs Consultant

Employer
Xplore Pharma
Location
Homeworking
Salary
Up to EUR0.00 per annum
Start date
27 Sep 2022
Closing date
27 Oct 2022

View more

Discipline
Regulatory Affairs
Hours
Full Time
Contract Type
Contract
Experience Level
Experienced (non-manager)
You need to sign in or create an account to save a job.

Job Details


This is an exciting rolling contract working in post-approval activities for the local French market on behalf of a Global Pharmaceutical company.

Responsibilities:

  • Review and Quality control of Post Authorization submission-related activities.
  • Advice to the client on France-specific requirements to support French regulatory activities.
  • Provide support on local regulations regarding aRMMs (additional risk minimization measures),
  • Review Labelling and Artwork
  • Review of the final published submission package
  • Notifying team of requests for information from Health Authority

Company

Xplore Life Science is a Life Science and Pharmaceutical Recruitment Consultancy providing an expert service, we are a challenger life science search firm. We place specialist talent within pharma, medical device, medical technology and consultancy businesses in the UK, Benelux, Switzerland (SECO License), Germany and the USA. Delivering on a contract, interim, permanent and retained search basis through a client-centric, transparent and lean recruitment process. Xplore are fully invested in our clients and candidates, focusing on delivering results for all parties, we are Dedicated to Life Science talent.

Find Us
Website
Telephone
+44 (0)203 865 5705
Location
154-158 Shoreditch High Street
London
England
E1 6HU
GB
You need to sign in or create an account to save a job.

Get job alerts

Create a job alert and receive personalised job recommendations straight to your inbox.

Create alert