Novartis Finland Oy is looking for Regulatory Affairs Manager
We have a wide portfolio with both new and established medicines products and you will be responsible for all aspects of regulatory work for a defined part of the products. You will work with CP, MRP and nationally approved products. The job will among others include submission of variation, translation of product information and work with and support Novartis global Regulatory Affairs. You will be part of cross functional teams and have close collaboration with marketing, medical, patient safety, supply chain, quality assurance and clinical trial monitoring team.
We expect you to have an educational background as a pharmacist or other relevant bio-medical background, and you have at least 2-3 years of regulatory experience in the pharmaceutical industry or with authorities. You have good analytical and systematic skills; and you demonstrate excellent communication skills – both written and verbal – and are fluent in both spoken and written English and local language(s).
The job requires in Regulatory Affairs requires that you
You will get the opportunity to work in a dynamic department with great colleagues and opportunities for professional and personal development. We are a collaborative team with high dedication and openness.
If you would like to know more about the job you can contact Head of Regulatory Affairs Anna Malmberg +358 (0)50 3101064; email@example.com (available days for calls: 28.6. from 15:00 – 16:00 or 20.7. from 14:00 – 15:00).
Novartis are an equal opportunities employer and welcome applications from all suitably qualified persons.
We kindly ask you to apply with an English version of your CV and if shortlisted you can expect a call from an international number.