- MSDS compilation for import clearance and poison item identification
- MSDS translation into Bahasa Malaysia in line with recent mandatory requirements by DOSH for all Health Institutions (Private & Government)
- Poisons identification housekeeping (Scheduled Poisons under the Poisons Act)
- Inter-departmental supply chain housekeeping support
- Identify check and assess product regulatory status according to regulatory requirements (medical devices poisons hazardous substances & flammables)
- Medical device certificates/licenses and Letters of Authorization files upkeep and re-organization
- Assist in checking product local labeling implementation
- Involvement in regulatory process improvements
- Involvement in regulatory database management and maintenance
- Assist the team with other ad-hoc regulatory matters
Requirements
- Background from Medical Bio-science Biomedical Science Biotechnology.
- Detail oriented.
- Organized good documentation practice.
- Basic ability to use Microsoft Word Excels Power Point.
- Good communication skills.
- Agile and adaptable.
- Good time management.
MSDS compilation for import clearance and poison item identificationMSDS translation into Bahasa Malaysia in line with recent mandatory requirements by DOSH for all Health Institutions (Private & Government)Poisons identification housekeeping (Scheduled Poisons under the Poisons Act)Inter-department...
- MSDS compilation for import clearance and poison item identification
- MSDS translation into Bahasa Malaysia in line with recent mandatory requirements by DOSH for all Health Institutions (Private & Government)
- Poisons identification housekeeping (Scheduled Poisons under the Poisons Act)
- Inter-departmental supply chain housekeeping support
- Identify check and assess product regulatory status according to regulatory requirements (medical devices poisons hazardous substances & flammables)
- Medical device certificates/licenses and Letters of Authorization files upkeep and re-organization
- Assist in checking product local labeling implementation
- Involvement in regulatory process improvements
- Involvement in regulatory database management and maintenance
- Assist the team with other ad-hoc regulatory matters
Requirements
- Background from Medical Bio-science Biomedical Science Biotechnology.
- Detail oriented.
- Organized good documentation practice.
- Basic ability to use Microsoft Word Excels Power Point.
- Good communication skills.
- Agile and adaptable.
- Good time management.
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