2 months ago

Regulatory Affairs Manager

Milton Keynes 60K - 72K Permanent

Job Reference: 934448

The Client

Our client is a fast growing UK Pharmaceutical company whose origins started over 12 years ago. They are at an exciting crossroads in their journey and are expecting their already established product portfolio to double in 2020. With a Board of Directors that have over 50 years combined experience in the healthcare sector, they have gained a reputation as a business that offers great value and service to their UK & International customers.

 

The Role

Due to continued growth, a fantastic opportunity has become available for an experienced Regulatory Affairs Manager to join the business. You will have high levels of responsibility and accountability, some of your key responsibilities will include: -

  • In-licensing and M&A due diligence
  • Maintenance of existing brands
  • Dossier development for future brands (eCTD)
  • Regulatory strategy development
  • Regulatory policy maintenance
  • Working with worldwide partners

 

The Candidate

It is likely the successful candidate will have the following:

  • Entrepreneurial attitude
  • Proactive & Progressive thinking
  • Strong Commercial Awareness
  • Regulatory expertise
  • Experience in dossier development
  • Have worked in small Pharma/start up environment
  • Experienced in converting non-UK to UK-ready dossiers (eCTD)
  • Knowledge of European & MHRA pharmaceutical legislation

 

How to apply

If the above sounds like your ideal role and you have the skills and attributes as listed above, please don’t hesitate to apply today. Please email a copy of your CV in a word document format to Gareth Loveys on garethl@harrislord.com 

Key words:  Regulatory Affairs, Pharmaceuticals, MHRA Regulations

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