Regulatory Affairs Postgraduate Program

Job description

Job Description

Are you interested to learn more about the pharmaceutical industry and Regulatory Affairs ? Do you want to start your career after your Master degree in Regulatory Affairs ? Would you like to experience work in a multicultural and diverse environment of a global healthcare company ? The Regulatory Affairs (RA) Program is an opportunity to discover the global functions of Drug Regulatory Affairs (DRA) and Regulatory Chemistry, Manufacturing and Controls (REG CMC). The candidates will be offered a Regulatory Affairs Postgraduate Program, consisting of rotation assignments within these departments.
Duration and start of employment: 2 years with an expected start date in January 2019
Deadline for application: end of June 2018
Interview: September/October 2018
Position Title

Regulatory Affairs Postgraduate Program

Desired profile

Minimum requirements

• Strong interest in Regulatory Affairs and Drug Development
• Completed MSc in Pharmaceuticals Sciences/Pharmacy/Life Science or equivalent and in Drug Regulatory Affairs (desirable)
• Fluency in English; additional languages, e. g. German or French are welcome
• Ready to expand your knowledge and are open minded with an international outlook
• Strong interpersonal skills, i.e. can demonstrate your ability to communicate well with people from a variety of backgrounds / cultures and at different hierarchy levels inside & outside the company
Job Type

Full Time
Country

Switzerland
Work Location

Basel
Functional Area

Interns/Students on Novartis Payroll
Division

Global Drug Development
Business Unit

REG AFFAIRS GDD
Employment Type

Internship
Company/Legal Entity

Novartis Pharma AG