Regulatory Affairs Manager (Myyntilupa-asiantuntija)

Job description

Job Description

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
• work independently
• pay attention to details
• are flexible but persistent and take the initiative to get the job done
• have a positive approach to life and manage to keep many balls in the air without losing either the big pictures or deadlines - even when things go fast.

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.

More information
If you would like to know more about the job you can contact Head of Regulatory Affairs Anna Malmberg +358 (0)50 3101064; (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.
Position Title

Regulatory Affairs Manager (Myyntilupa-asiantuntija)

Desired profile

Minimum requirements

please see above
Job Type

Full Time
Country

Finland
Work Location

Espoo
Functional Area

Research & Development
Division

Global Drug Development
Business Unit

REG AFFAIRS GDD
Employment Type

Regular
Company/Legal Entity

NOV FIN