- Business Nature: Medical Device R&D and Manufacturing
- Location: Johor Bahru
- To monitor the regulatory process for products that require government approval.
- To coordinate organizational examinations and contract facilities.
- To develop procedures to ensure regulatory compliance.
- To conduct audit ISO 9001 and ISO 13485 for medical equipment quality system.
- Bachelor/Master Degree in Biology, Biotech, Biomedical Engineering or its equivalent.
- 3-5 years experience in related field.
- Familiar with ISO 13485 and overseas and local regulatory standards.
- Good communication and good command of English.