Do you have experience in European Regulatory Affairs? Would you like to work in the varied and fast-paced environment of generic products? If so, we're looking for someone like you...
Teva is recruiting a Senior Regulatory Affairs Associate to work within the European Regulatory Affairs Team, based at our office in Harlow, Essex. You will work in a large team of regulatory affairs professionals, working in a key hub of Teva’s Regulatory Affairs organisation. Almost 200 people, across multiple functions, are based in Harlow, working collaboratively for Teva, one of the biggest pharmaceutical companies in the UK and among the top 15 pharmaceutical companies in the world.
The focus of the role will be on the submission of new generic Marketing Authorisation Applications (MAAs) for a wide variety of products and dosage forms for retail use, registered via the Decentralised or Mutual Recognition Procedures. This high profile role will mean you working with third party partners, portfolio, local business units and a whole host of other stakeholders. Due to the varied nature of the role, there will be the opportunity for exposure to a wide range of regulatory issues and procedures.
If you have significant EU Regulatory Affairs experience and would like to work in a fast paced and dynamic environment, then we’d love to hear from you!