Regulatory Affairs Specialist

at  Novo Nordisk

Regulatory Affairs Specialist
Category: Reg Affairs & Safety Pharmacovigilance
Location:Santiago, Región Metropolitana, CL
Do you have experience working with biologics and supporting the introduction of new treatments to the market? Would you like to be part of a dynamic team and make it possible to introduce innovative biological molecules for the first time in the country? Join us and be part of this exciting challenge! We are looking for a Regulatory Affairs Specialist to join our team in Chile. The position provides you the opportunity to work in a high performing team to contribute directly towards the business results while creating values for the patients. If that sounds like you, read on and apply today for a life-changing career.

QUALIFICATIONS

We realize that few people are experts at everything. But if you can nod your head at the following attributes then you could be the person we are looking for:

• University degree in Pharmacy (degree validated in Chile).
• Minimum 4 years’ experience in the Regulatory Affairs area for the pharmaceutical industry.
• Experience in registration and/or modifications of biotechnological products, including management of the GICONA regulatory platform.
• Experience with regulatory systems and packaging material management is desirable.
• Fluent in oral and written English.

Additionally, to be successful in this role, you should have:

• Excellent attention to details while working on multiple tasks
• Ability to work effectively with cross-functional teams, to ensure regulatory compliance and delivering excellent performance and results
• Flexibility to adapt to changing regulatory environments and requirements, ensuring continuous compliance and successful product lifecycle management

• Excellent attention to details while working on multiple tasks
• Ability to work effectively with cross-functional teams, to ensure regulatory compliance and delivering excellent performance and results
• Flexibility to adapt to changing regulatory environments and requirements, ensuring continuous compliance and successful product lifecycle managemen