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GENERAL SUMMARY OF ROLE:
This role will be responsible for all the domestic and regional regulatory affairs (RA), including but not limited to NDAs, variations and registration renewals in Singapore and Asian countries.
She (or he) shall also be responsible for establishing domestic and regional pharmacovigilance for the products.
Responsibilities:
. Responsible for the preparation and documentation of regulatory submissions to government agencies.
. Works on problems of diverse scope where analysis of situations or data requires a review of identifiable factors.
. Exercises judgement within generally definend other corporate groups.
. Monitors FDA and other agency laws and regulations, and provides recommendations and assistance to ensure company compliance.
. Direct certification application activities including sending and tracking certification letters. Maintain tracking log, and supply global registration requests.
. Provides metrics for regulatory management reporting and helps to identify areas for further monitoring for global product development system (GPDS) improvements.
. Track global registration status for project teams and new products. Log, track, and prepare report from eGPS system.
. Brings Regulatory Affairs questions/issues to the attention of RA management.
. Preparing responses to agency's questions with good writing and communication skills.
. Performs other related duties and assignments as required.
EDUCATION AND EXPERIENCE
SKILLS/KNOWLEDGE/ABILITIES/BEHAVIOUR TRAITS
. Project strong initiatives to establish the operating procedures for a new start-up organization.
. Detail-mindset, responsible, well-organized
. Strong communication and interpersonal skill in shared office environment.
. Pro-active and positive mindset
. Able to Prioritize tasks and workload
If you are interested in the position, do kindly drop your most updated resume to (Attn: Regulatory Affairs)
Thank You.
Leon Leong De Cong
R1551708
EA License: 99C4599
Recruit Express Pte Ltd
Date Posted: 19/08/2025
Job ID: 124174025