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Teva Senior Manager - Regulatory Affairs Innovative Medicines Europe 
United Kingdom, England 
910494501

25.06.2024
A day in the life of a Senior Manager Regulatory Affairs...
  • You will develop regulatory strategies during development, approval and post approval phases for submissions to EU Competent Authorities. You may also have the opportunity to do this on a Global scale in the capacity of Global Regulatory Lead.
  • You will obtain regulatory approvals and other feed-back 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 to ensure that the registrations for existing marketed products are maintained.
  • You will provide regulatory guidance to cross-functional teams within Teva.

Do you have?

  • A strong Scientific background with a BSc degree in Life or Pharmaceutical/Healthcare Sciences – ideally with a MSc or PhD
  • Substantial European regulatory affairs experience (must have)
  • Experience in Clinical Trial Applications in the EU (must have)
  • Innovative Medicine experience in Immunology and/or Oncology and/or Gastroenterology and/or Respiratoy therapeutic areas is a significant advantage, but we are open to consider any therapeutic area.
  • Strong leadership and interpersonal skills

Are you?

  • An excellent written and verbal communicator and confident presenting/communicating with local and global groups
  • Able to work under pressure to meet tight deadlines
  • A strategic thinker with strong problem solving skills
Enjoy a more rewarding choice
  • Enjoying time with your families (25 days of annual leave, Hybrid approach to home working, Pension scheme, car or car allowance)
  • Looking after your health (Life & Critical Illness Insurance, Private health insurance for you and your family, Sports and Health Programme – including health days and nutritional counselling, On-site Canteen)
  • Recognizing your value (Recognition programs to reward our employees with our company bonus scheme)
  • Boosting your potential (Virtual Learning Centre)
  • Well-being and D&I focused company
Sub Function
Medical Regulatory Affairs
Reports To

Senior Director, EU Regulatory Affairs Branded

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