Quality Engineer II
Job Duties:
Develops and executes plans for quality and control to ensure manufacturing continuity and product conformance.
Leads investigations into production and customer-facing quality issues to identify root cause, implement corrective and preventative actions, and monitor effectiveness
Monitors and analyses product performance of medical devices using a statistical and risk-based approach. Considers any quality, compliance, customer, and business risks.
Performs hands-on troubleshooting of customer returned devices and manufacturing nonconformities and completes associated technical documentation
Develops tools to communicate complex technical problems and solutions to a variety of audiences within the organization
Proficient in project management, data analysis, root cause analysis, communication, and risk determination
Ensure compliance with the company's Quality System policies and procedures and applicable external requirements and standards, including FDA, ISO 13485, and other worldwide regulatory agencies as pertaining to medical devices.
Minimum Requirements:
Bachelor's degree in Engineering
3 years of relevant experience in a regulated industry (FDA environment preferred)
Knowledgeable of FDA regulations, 21 CFR part 820 and Part 803 and ISO 13485 standard
Strong verbal / written communication, with the ability to work effectively in cross-functional teams
Custom Fields:
Name: Supervisory Org
Value: Quality Operations - Sustaining Engineering 3(Marylinda Cordova)-60003870
Name: Workspace
Value: None
Name: System Access Required
Value: Yes
Name: Work Desk Phone Number Required
Value: No
Name: Badge ID Required
Value: Yes
Name: Invoice Type
Value: USA-ARL-Staffing-USD
Name: Remote Worker
Value: No
Name: Worker Time Type
Value: Full Time
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