Job Description

Responsibilities:

-To fully assist in product (medical device) registration and regulatory compliance with relevant government bodies for group of companies

-To assist in implementation of ISO and GDPMD standard for group of companies

-To assist in all administration jobs related to the regulatory affairs and quality assurance matters

-Lead product registration, system certification, certificate renewal, and replacement applications in line with company plans.

-Oversee registration progress, liaise with government and industry departments, resolve issues, and ensure timely approvals.

-Continuously monitor and interpret regulatory changes, providing updates to management and teams.

Requirements:

- Minimum Diploma / Degree in Business Administration/Biomedical or equivalent

-At least 1 year of related experience in regulatory affairs, preferably under medical device industry

-Good interpersonal and communication.

Job Type: Full-time

Pay: RM2,200.00 - RM3,000.00 per month

Benefits:

Health insurance Maternity leave Opportunities for promotion Professional development
Work Location: In person