Responsibilities:
- Prepare and compile registration documents according to country-specific guidelines.
- Consolidate raw data, reference information, and technical specifications.
- Assist in preparing GMP-related requirements.
- Coordinate with various departments and customers to gather registration requirements.
- Liaise with relevant authorities (NEA, SCDF, SPF, HSA and MOM) on licensing, compliance and other legislative matters.
- Evaluate new products if license is required according to local regulations.
- Prepare Safety Data Sheet (SDS) and GHS labels in accordance to Globally Harmonized System (GHS) standards.
- Manage registration sample requests, receipts and dispatch by proper recording and monitoring and storage.
Requirements:
- Min NITEC / Diploma in Applied Chemistry, Biomedical Science, Biotechnology or any other science-related course
- Experience in lab testing is an advantage, but entry-level are welcome too (training provided)
- Posses good analytical skills, meticulous & organised
How to Apply:
Interested candidates, please submit your updated resume by using Apply Now button
**We regret to inform that only shortlisted candidates will be informed.**
Tan Zhi Ning
Registration Number: R23116771
EA License No: 18C9027
