Regulatory Affairs Director

18 hours ago


Harlow, Essex, United Kingdom Teva Pharmaceuticals Full time
Job Description

We are seeking a highly skilled Regulatory Affairs Director to join our Global Regulatory Affairs – Innovative Medicines (Europe) team at Teva Pharmaceuticals.

This is an exciting opportunity to work with key innovative products part of our Pivot to Growth strategy. You will be responsible for developing regulatory strategies during development, approval and post approval phases for submissions to EU Competent Authorities.

A Day in the Life

  • You will obtain regulatory approvals and other feedback or decisions from European Competent Authorities during development of innovative medicinal products.
  • You will support Clinical Trial Applications under the new Clinical Trials Regulation.
  • You will obtain registrations for innovative medicinal products, in the EU and ensure that the registrations for existing marketed products are maintained.
  • You will provide regulatory guidance to cross-functional teams within Teva.

About You

  • You have a strong scientific background with a BSc degree in Life or Pharmaceutical/Healthcare Sciences – ideally with a MSc or PhD.
  • You have substantial European regulatory affairs experience.
  • You have experience in Clinical Trial Applications in the EU.
  • Innovative Medicine experience in Immunology and/or Oncology and/or Gastroenterology and/or Respiratory therapeutic areas is a significant advantage.

Benefits

  • You will enjoy a competitive salary range of £80,000 - £110,000 per annum, depending on your experience.
  • You will also receive 25 days of annual leave, a hybrid approach to home working, pension scheme, car or car allowance, life & critical illness insurance, private health insurance for you and your family, sports and health programme, on-site canteen, recognition programs, virtual learning centre, well-being and D&I focused company.


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