- Jalan Kerinchi Kuala Lumpur WP Kuala Lumpur Malaysia 59200

KL City, WP Kuala Lumpur
Working Location
Job Description
Requirements
Qualification
Strong command of English and Bahasa Malaysia (verbal and written)
Strong understanding of Malaysia and Indonesia regulations.
Ability to ensure accuracy in documentation, packaging, and product compliance.
Ability to manage multiple tasks, prioritize tasks effectively, and meet deadlines.
Responsibilities
Main responsibilities:
Prepare, compile, submit and maintain product registrations related to registration, renewal, and license amendments of medical devices, till approval process with the Malaysian Medical Device Authority (MDA) & Ministry of Health (Kemenkes).
Monitor submission status and support timely responses to deficiency letters and regulatory authority requests, ensuring accurate documentation of all interactions.
Liaise with regulatory authorities, conformity assessment bodies (CAB), and other relevant authorities.
To keep abreast of local regulatory updates, guidelines and new regulations, and its implementation.
Ensure that the product, packaging, and labeling of the current and new products comply with the regulatory requirements.
Perform change impact assessment for Malaysia and Indonesia.
Perform advertisement and promotional material review in accordance with local regulations.Other tasks as assigned.
Benefits
Skills
LRT - KERINCHI
0.6 km
LRT - UNIVERSITI
0.6 km
KTM - ANGKASAPURI
0.9 km
KTM - ABDULLAH HUKUM
1.2 km
LRT - ABDULLAH HUKUM
1.2 km
KTM - MID VALLEY
1.7 km
KTM - PANTAI DALAM
1.7 km
KTM - SEPUTEH
1.8 km
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