Regulatory Affairs Executive

Product registration with NPRA

Responsibilities

• Manage regulatory affairs including product registration and legal requirements.
• Prepare product classification, labeling and maintain SDS (safety data sheet) in compliance with CLASS regulation.
• Scheduled Waste Management
• Timely reporting to relevant authorities (CIMS, eSWIS, CWC, Feed Act & Poison Act, etc.).
• Work closely with manufacturers / principals / suppliers to prepare and obtain relevant documentation and information on products complying to Legal Requirements.
• Conduct training from time to time to staff on necessary skills and knowledge to ensure regulatory compliance in their daily work activities.
• Develop work procedures whenever necessary to ensure regulatory compliance in their daily work activities.
• Maintain and update the Product Master List, SDS for all current active products.
• Check Shipping Schedule and apply necessary Import / Export Permits / Approvals to facilitate smooth exportation / importation processes.

Qualifications

• Degree in Pharmacist or Chemistry with RA experience will be good
• At least 2 – 3 years’ experience in the Chemicals industry / distribution environment.
• Possession of a valid pharmacist license will be an added advantage

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