Regulatory Affairs Manager

2 weeks ago

Harlow, Essex, United Kingdom Tevapharm Full time
Join Our Team as a Regulatory Affairs Professional

We are seeking a highly skilled Regulatory Affairs Professional to join our team at Teva Pharmaceuticals. As a key member of our Global Regulatory Affairs – Innovative Medicines (Europe) team, you will play a critical role in developing regulatory strategies for innovative medicinal products.

Your responsibilities will include:

  • Developing regulatory strategies for submissions to EU Competent Authorities
  • Obtaining regulatory approvals and feedback from European Competent Authorities
  • Supporting Clinical Trial Applications under the new Clinical Trials Regulation
  • Providing regulatory guidance to cross-functional teams within Teva

Requirements:

  • BSc degree in Life or Pharmaceutical/Healthcare Sciences
  • Substantial European regulatory affairs experience
  • Experience in Clinical Trial Applications in the EU
  • Innovative Medicine experience in Immunology and/or Oncology and/or Gastroenterology and/or Respiratory therapeutic areas

We offer a competitive salary and benefits package, including:

  • 25 days of annual leave
  • Hybrid approach to home working
  • Pension scheme
  • Car or car allowance

Apply now to become a part of our team and contribute to the development of innovative medicinal products.

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