REGULATORY AFFAIRS ASSOCIATE
About this position
The Regulatory Affairs Associate is responsible for ensuring compliance with regulatory requirements, preparing and submitting necessary documentation, and supporting pharmacovigilance activities.
Responsibilities
• Perform appropriate regulatory evaluations in compliance with relevant requirements
• Prepare, submit and monitor license registration, variations, GMP clearance, and renewal
• Prepare and submit regulatory reports in compliance with relevant regulations
• Perform pharmacovigilance activities e.g., Adverse event reporting
• Update and maintain regulatory databases.
• Support FDA submission of promotional materials
• Other regulatory duties as assigned by the supervisor
Requirements
• Bachelor's degree in pharmaceutical science with an active license
• Minimum 3 years of experiences in regulatory affairs
• Experience in bioequivalence study or pharmacovigilance area will be an advantage
• Proactive, quick learner, well organized and prioritized to fulfill requirements and timeline
• Able to achieve multiple tasks under pressure or committed timelines
• Able to work independently, at the same time a good team player
• Good interpersonal and effective communication skills
• Good command in English