About this role
Maintain the Quality Management System in compliance with ISO 13485 and lead CAPA investigations and root cause analysis. Collaborate with cross-functional teams to manage risk, perform audits, and drive continuous improvement in manufacturing processes.
Requires a Bachelor's degree in Engineering or Life Sciences with 3-8 years of quality engineering experience in the medical device or healthcare industry. Must have strong knowledge of FDA regulations, ISO standards, and validation activities.
What they're looking for
ISO 13485FDA 21 CFR Part 820ISO 14971CAPARoot Cause AnalysisInternal AuditingRisk ManagementGMP
Frequently asked questions
What does a Quality Engineer (Medical Devices) at Jabil do?
Maintain the Quality Management System in compliance with ISO 13485 and lead CAPA investigations and root cause analysis. Collaborate with cross-functional teams to manage risk, perform audits, and drive continuous improvement in manufacturing processes. Requires a Bachelor's degree in Engineering o…
What skills does this Quality Engineer (Medical Devices) role need?
Key skills for this role include ISO 13485, FDA 21 CFR Part 820, ISO 14971, CAPA, Root Cause Analysis, Internal Auditing.
How much does a Quality Engineer (Medical Devices) at Jabil pay?
The employer did not list a salary for this role. Most similar Singapore roles publish their band on the job page.
Is this Quality Engineer (Medical Devices) role remote, hybrid, or on-site?
This role is on-site, based in Singapore.
How do I apply for this Quality Engineer (Medical Devices) role?
You can apply directly on Jabil's careers page. ApplyLah can tailor your résumé and cover letter to this exact role in seconds first.