Akkodis Group Nordics · 1 day ago
Quality Engineer III
Akkodis is seeking a Quality Engineer III for a Contract with a client in Arden Hills, MN. The role involves leading cross-functional teams to investigate product performance issues and implementing corrective actions.
Embedded SystemsSoftware
Responsibilities
Lead cross-functional teams to investigate complex product performance issues and implement effective corrective and preventive actions (CAPAs)
Conduct root cause analysis using structured problem-solving tools such as DMAIC, 5 Whys, and Cause & Effect diagrams
Create and maintain detailed investigation documentation following Good Documentation Practices and Quality System requirements
Collaborate with R&D, Regulatory, Manufacturing, and other teams to resolve technical issues and ensure compliance with medical device regulations
Present investigation updates to senior leadership and provide technical guidance to other engineers and teams
Support continuous improvement initiatives within Design Quality, risk management, and new product development processes
Qualification
Required
Bachelor's degree in engineering or a related discipline
4+ years of relevant experience in Quality Engineering within the medical device industry
Strong expertise in root cause analysis and corrective/preventive actions (CAPA) using structured problem-solving tools (DMAIC, 5 Whys, etc.)
Proven experience with Quality System Regulations, ISO 13485 standards, and compliance in a regulated medical device environment
Benefits
Medical
Dental
Vision
Life insurance
Short-term disability
Additional voluntary benefits
EAP program
Commuter benefits
401K plan
Paid Sick Leave
Holiday pay
Company
Akkodis Group Nordics
Akkodis Group Nordics, operates as a specialized tech cluster, combining expertise in Digital Engineering and Edge Technology.
Funding
Current Stage
Late StageTotal Funding
unknownKey Investors
Reiten & Co
2020-03-16Acquired
2009-05-01Private Equity
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