Job description Location – Tuas
Working hours /day – 8.30am to 5.30pm/5days
#ISO 13485 is the international Quality Management System (QMS) standard specifically designed for the medical device and medical technology industry.
Responsibilities - Manage Project schedule and ensure work performed with desired quality and meeting design specification, regulatory standard IS13485 and FDA 21 CFR Part 820
- Ensure customer’s specification and requirements understood and executed so as to provide good engineering solutions
- Prepare Engineering documents which include process , set up plan and Quality plan
Requirements - Degree in Mechnical Engineering or EEE with 1 year experience
- Diploma in Mechnical Engineering or EEE with 2 years experience
Project Management Knowledge: Solid understanding of project management principles and practices, including sch...