About the Role
Responsibilities / Essential Functions:
-Serves as the key regulatory person by providing necessary documents to the Office of Regulatory Affairs (ORA) or the Food and Drug Administration (FDA) during initial or renewal applications or when there are regulatory inspections or queries.
-Oversees the whole process of artwork preparation of packaging and promotional materials by coordinating with the Product Management Group (PMG) and various corporate enablers when there are new or alternatively-sourced products or whenever a revision is needed.
-Participates in the continuous training in the Division by giving technical lectures to the new and existing field force and other personnel whenever there are new hires or when a refresher training is needed.
-Processes all requirements by trade partners and hospital institutions for product bidding and formulary inclusion. Secures and monitors valid and authenticated documents such as CPR, COA and CGMP for each product and facilitates third party assay testing and other necessary inclusion requirements.
-Maintains current registration, studies existing and new legislation, anticipates legislation, and advises management on needed actions.
PRC ID and Certificate
Notarized Employment Contract
Annual Health Status (Latest Medical Certificate)
Latest NBI/Police Clearance
PSA Birth Certificate
Certificate of Employment from previous employer
SSS MDF Form
PhilHealth ID/ MDR Form
PAG IBIG ID/ MDF Form
Marriage Contract if Married