The opportunity
We are recruiting for a Manager or Senior Manager – Regulatory Affairs to work within the Global Regulatory Affairs – Innovative Medicines (Europe) team. You will be working with key Innovative products part of Teva´s Pivot to Growth strategy.
Do you know that our Harlow office is the Centre of Excellence (CoE) for Regulatory Affairs within Teva, with teams covering both European and global licensing for medicines and over-the-counter (OTC) products? The site is conveniently located half an hour commute from central London. We have a hybrid approach to home working!
A day in the life of a Manager/Senior Manager Regulatory Affairs…
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.
