Teva Manager/Senior Manager - Regulatory Affairs Innovative Medicines Europe 

United Kingdom, England 

551874041

• You will develop regulatory strategies during development, approval and post approval phases for submissions to EU Competent Authorities. Depending on your experience 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 Respiratory therapeutic areas is a significant advantage, but we are open to consider any therapeutic area
• Experience with Medical Devices and the Medical Device Regulation would also be an advantage
• Strong leadership and interpersonal skills
  

• 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
  

• 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
  

Medical Regulatory Affairs

Associate Director, EU Regulatory Affairs Innovative Medicines

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