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

Or

Diploma in Mechnical Engineering or EEE with 2 years experience

Project Management Knowledge: Solid understanding of project management principles and practices, including scheduling, resource allocation, and progress tracking.

send your resume to [email protected]