About this role

  • Posted on

  • Location

    Berkshire, Slough

  • Salary

    £60000 - £80000 per annum

  • Type

    Permanent

  • Division

    Pharmaceutical Regulatory Affairs Jobs

  • Reference

    BB - 12758.2_1599119679

  • Start date

    ASAP

  • Managing this role

Executive Consultant

Brieuc Baeckeroot

+44 203 8540 263

brieuc.baeckeroot@xplorelifescience.com

Source Group International GmbH, Bosch 106, 6331 Hunenberg, Switzerland

Description

The Brexit is due by the end of the year and will bring its adaptation. The companies need to anticipate, adapt in order to avoid being left behind by the impact it can have.
The role has its part of the unknown and divided in two-part which is where it creates a really interesting and challenging role.

In the first part, you will serve as a liaison between the group and the MHRA. You will give an overview of the changes, during the transition linked to the Brexit in order to minimise the impact for the Regulatory team.
In the other part of the role, you will advise the development teams on the Regulatory strategy and procedures. This will be for Biologic and Pharmaceutical products.

This will be challenging by the unknown that offers the Brexit and you will play a key role within the teams. You will develop strong knowledge for the post Brexit situation and act as an expert in the future.

Your task:

  • Alongside the development team, you will advise the local strategy & processes to adopt.
  • Working across regions to provide support in order for them to deliver the product algin with the strategy
  • Being the main regulatory liaison between MHRA and the group.
  • Provide the resources, knowledge in order to adapt the right strategy and operational regulatory input across the teams.

Your experience:

  • Several years of experience in Regulatory Affairs ideally:
  • Worked within the Biotech and Pharmaceutical products
  • Got strong knowledge of the Development phases to the submission and registration of the product
  • Worked on a local level with the MHRA
  • Able to work in cross-functional projects

This is a role where you will be challenged, you will need to have an open mindset to be able to come with solutions for the regulatory teams. If you are up for a new challenge, with a part of the unknown contact me.

Contact:

Feel free to reach me even if the position is not exactly what you are looking for.
Please share it with your network or any person you think you might be interested in.

You can send me your CV, Resume with your contact details through the link OR you can contact me on Linkedin.

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