Role & Responsibilities:
- Prepare registration documents according to country specific guidelines for submission to legislation authorities.
- Consolidate and compile raw data, reference information and product technical specifications.
- Assist in the preparation of GMP related requirements
- Coordinate with laboratory, production and other relevant departments to gather registration requirements.
- Coordinate with customers on registration requirements.
- Arrange endorsement for regulatory documents.
- 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.
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
