More jobs:
Quality Engineer
Remote / Online - Candidates ideally in
Irvine, Orange County, California, 92618, USA
Listed on 2026-02-12
Irvine, Orange County, California, 92618, USA
Listing for:
Aequor Technologies LLC
Full Time, Remote/Work from Home
position Listed on 2026-02-12
Job specializations:
-
Engineering
Quality Engineering -
Quality Assurance - QA/QC
Quality Engineering
Job Description & How to Apply Below
Description:
The Quality Engineer is responsible for maintaining quality and control of manufacturing processes and post-market performance of medical devices. Responsibilities include collaborating with internal and external stakeholders to achieve company objectives, leading technical root cause investigations, developing and executing risk-based decisions, resolving and documenting customer complaint and manufacturing investigations, and representing Quality in cross-functional projects.
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
2 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
Bachelor s degree in Engineering
Custom Fields:
Name:
Badge
Value:
Yes
Name:
Supervisory Org
Value:
Quality Operations - Sustaining Engineer 2(Kevin Bellows)
- Name:
Remote Worker
Value:
No
Name:
Work Desk Phone Number Required
Value:
Yes
Name:
System Access Required
Value:
Yes
Name:
Invoice Type
Value: USA-ARL-Staffing-USD
Name:
Workspace
Value:
None
Name:
Worker Time Type
Value:
Full Time
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