Role & Responsibilities
1. Prepare registration documents according to country specific guidelines for submission to legislation authorities.
2. Consolidate and compile raw data, reference information and product technical specifications.
3. Assist in the preparation of GMP related requirements
4. Coordinate with laboratory, production and other relevant departments to gather registration requirements.
5. Coordinate with customers on registration requirements.
6. Arrange endorsement for regulatory documents.
7. Liaise with relevant authorities (NEA, SCDF, SPF, HSA and MOM) on licensing, compliance and other legislative matters.
8. Evaluate new products if license is required according to local regulations.
9. Prepare Safety Data Sheet (SDS) and GHS labels in accordance to Globally Harmonized System (GHS) standards.
10. Manage registration sample requests, receipts and dispatch by proper recording and monitoring and storage.
Role Requirements:
· Diploma / Nitec in applied Chemistry, Biomedical Science, Biotechnology or any other science related discipline
· Experience in lab testing is an advantage
Working Hours:
· Monday – Friday: 8.15am-5.30pm
Benefits:
· Transport provided at Lakeside & Boon Lay MRT station
· Medical Insurance upon confirmation
· AWS and profit sharing upon eligibility
