Regulatory Affairs Specialist CIS
750 million. That's how many lives our products touch. And while we're proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people's lives?
We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you're given opportunities to explore the power of digital and data. Where you're empowered to risk failure by taking smart risks. And where you're surrounded by people who share your determination to tackle the world's toughest medical challenges.
Currently, we are looking for Regulatory Affairs Specialist CIS for further development and support of our activities in Ukraine
Location: Kyiv
Responsibilities
- Support of medicinal products registration in CIS countries and marketing authorizations maintenance in accordance with local regulations and company strategy.
- Development and management of the country specific normative documents (product information, production artworks, etc.).
- Maintaining of internal databases.
- Communication with external stakeholders i.e. service providers and relevant health authorities.
Requirements:
- University degree in Life science or Pharmacy
- Upper-intermediate English with knowledge of medical terminology
- Minimum 1 year of experience in Drug Regulatory Affairs
You will receive:
- Competitive salary and bonus levels;
- Medical and life insurance;
- Work in an international innovative company;
- Be part of a mission to reimagine medicine to improve and extend people's lives
Iryna Kshanovska
Novartis Pharma Services AG Перевірена
