Regulatory Affairs Executive – Southampton, UK

As a Regulatory Affairs Executive you will assist in regulatory activities relating to the UK and Irish division, ensuring compliance of all medicinal products.

Your main responsibilities will include:

  • Ensure compliance of medicinal products to UK, IMB and EU legislations.
  • Facilitate the process of submissions relating to MAA in the UK and Ireland and coordinate the submission and responses as appropriate for European procedures.
  • Provide expert advice to other departments in relation to UK and Irish regulations.
  • Provide input and coordinate product package and final artwork.
  • Ensure compliance with internal and external SOPs.
  • Ensure all paper and electronic documents are correctly filed.

The ideal candidate for this Regulatory Affairs Executive position will have the following experience and skills:

  • Previous experience within regulatory affairs in the pharmaceutical industry essential.
  • Post marketing maintenance experience essential.
  • Experience liaising with the MHRA and IMB required.
  • Excellent attention to detail.
  • Excellent written and verbal communication.
  • Computer literate.

 

 Apply Now

For more information, or to apply for this Regulatory Affairs Executive position, please contact Meera on 01438 743 047 or email mpattni@ckregulatory.com.

Alternatively, click here to apply for this Regulatory Affairs Executive role online now.

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