TAPI's commercial products regulatory affairs (RA) unit is hiring a regulatory affairs associate to support its global Active pharmaceutical ingredient (API) activity. (Temporary position)
The job includes:
Support the lifecycle management of APIs from RA perspective.
Coordinate Drug master file (DMF) preparation and related activities for new market submission.
Respond to deficiency letters and coordinate related activities.
Submit updates and variation of changes according to the regulatory requirement.
Evaluate change requests from RA view.
Support customers regarding service requests
• Master's degree in chemistry/biochemistry – must
• PhD – an advantage
• Global experience / RA experience – an advantage
• Fluent English - must
• Full time position in our Petach Tikva HQ
For applying your CV: