Regulatory Affairs Associate

Date Posted: September 11, 2020

Job Location: Paranaque City

Job Description:

Position Objective:  Sr. Regulatory Affairs Executive is responsible for preparations and submissions of CLIDP applications, renewals, GMP applications, LTO inclusions, Batch Notifications, CLIDP re-issuances and compilation of requirements of products for Assay Testing of Regulatory Affairs. This is a desk-based role, involving the close study of scientific and legal documents.


• Preferrably a health related course graduate   
• With good communication skills: written and oral
• Knows how to operate Microsoft Office (MS Word, Excel, Powerpoint, Outlook), PDF (Nitro Pro, Adobe etc).
• With good administrative / organizational skills
• With good relational skills; has high capability to handle foreign accounts