Editorial summary

The company, a leading medical device manufacturer located in the East, is seeking multiple Senior/Quality Engineers to join its expanding team. The role involves supporting quality activities across manufacturing processes and products, performing inspections, testing, verification, and process evaluations, and analyzing quality data to identify trends and support investigations. Desired qualifications include experience in medical device QA, familiarity with GMP/ISO 13485, and strong analytical skills. Compensation is up to 6,000 per month.

This summary is AI-generated and may contain inaccuracies. Please refer to the full job description below.

Job description

[This job https://singapore.job-q.com/jobs/detail/senior-quality-engineer-medical-device-manufacturing-east-41877 first appeared in Job-Q.com on 07 Nov 2026]

Our client is one of the leading players in the medical devices manufacturing sector. Due to their current expansion plan, they are looking for a multiple headcounts of Senior/Quality Engineer to join their team, in hopes of developing the current high performing team. They are located in the East area.

Job Responsibilities:

• Support quality activities across manufacturing processes, products, and daily operations.
• Perform or support product inspection, testing, verification, and process evaluation activities.
• Gather and analyse quality data to identify trends, support investigations, and improve process performance.
• Investigate quality concerns raised by customers, production teams, and internal stakeholders, and assist in identifying root causes.
• Coordinate follow-up actions for customer complaints, non-conformities, and process-related issues.
• Assist in implementing corrective and preventive actions to address recurring quality issues.
• Participate in risk assessment, failure analysis, PFMEA, and other quality improvement activities.
• Work closely with Engineering, Manufacturing, Operations, and other teams to resolve quality issues and improve processes.
• Support Quality Management System requirements and participate in internal, customer, supplier, and external audits.
• Maintain quality records, procedures, work instructions, reports, and other controlled documentation.
• Participate in continuous improvement projects to enhance product quality, process efficiency, and reliability.
• Perform any ad-hoc duties as assigned.

Requirements:

• Min Diploma or Degree in Engineering, Science, or a related technical field.
• Min 3-5 years of relevant experience in Quality Engineering/QMS.
• Exposure to regulated environments or ISO 13485 will be an advantage.
• Familiar with quality and problem-solving tools such as 8D, 5-Why, etc. will be advantageous.

Interested candidates who wish to apply for the advertised position, please click APPLY NOW or email an updated copy of your resume/cv.

We regret that only shortlisted candidate will be notified.

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