Specialist, Regulatory Affairs FDF

Supports the Regulatory Affairs-FDF Team by contributing to regulatory activities and objectives, including product dossiers, variation packages, and regulatory procedures.

Requirements

• Academic degree in Pharmacy, Chemistry, or Biomedical field
• 3-5 years of experience in regulatory affairs and/or relevant health registration environments of medicinal products
• Familiarity with registration procedures and requirements in the global environment
• Professional training in Regulatory Affairs field
• Accuracy, creativity, trouble-shooting capability
• Good communication skills, including English language proficiency

Benefits

• Truly global work environment
• High performance culture
• Ability to make a difference
• Best in class compensation