DHR Clerk

QUASAR MEDICAL (SINGAPORE) PTE. LTD.; Singapore; On-site; SGD 20,000 - 60,000; Full time

Job summary

A leading medical device company in Singapore seeks an individual to support day-to-day production activities and health and safety programs. The role involves ensuring cleanliness through 6S, participating in improvement projects, and adhering to ISO13485, GMP, and FDA regulations. Candidates should have at least 1 year of assembly experience in the medical device industry and possess excellent communication skills.

Qualifications

• 1+ years of assembly experience, preferably in the medical device industry.
• Knowledgeable in GMP, ISO, cleanroom procedures, and documentation.

Responsibilities

• Involve and support Health and Safety programs.
• Ensure cleanliness of working place by performing 6S.
• Involve in Production/Engineering improvement projects.

Skills

Excellent communication Skills

Computer literate

Education

Primary or GCE “N” level or higher

Job description

Essential Duties and Responsibilities: Include the following. Other duties may be assigned.

• Involve and support Health and Safety programs (DWB, BBS, H&S meetings).
• Ensure cleanliness of working place by performing 6S
• Involve and support in Production/ Engineering improvement project (Kaizen).
• Support day-to-day production activities
• Work with supervisor and follow up status of DHR base on Shared Master Delivery Schedule file to meet the lead time for DHR reviewing
• Work with supervisor to align and meet the target for DHR KPI with Quality
• Work with supervisor to develop process improvements to improve workflow efficiency, schedule and strategy to avoid delays.
• Communicate production GDP updates and errors to Supervisor on regular basis
• Maintain and comply with ISO13485, GMP and FDA regulations

Education/Experience and Qualifications:

• Primary or GCE “N” level or higher, with 1+ years of assembly experience, preferably in the medical device industry.
• Excellent communication Skills
• Computer literate
• Knowledgeable in GMP, ISO, cleanroom procedures, and documentation