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Quality Engineer I
LaborieUnited Statesfull_timeVerifiedPosted 26 Aug 2025
About the role
We believe that great healthcare is an essential safeguard of human dignity.At Laborie, we know the work we do matters – it’s what fuels our motivation and contributes to our success. If you’re ready to make a positive impact in the lives of patients across the globe, we’d like to meet you. We support and empower our employees to grow their careers in an environment that encourages a sense of belonging and a connection to doing good. We’re not afraid to roll up our sleeves to make our goals a reality and work together to solve for our customers. We reward and recognize our employees based on our values of Aspire to Greatness, Respect All, Own It, Working Together, Persist with Passion. Who We’re Looking For:As a key member of the Quality team, the Quality Engineer I will be responsible for ensuring that the technical regulatory and quality requirements are met for products throughout their product life cycle. About the Role:
- Provide quality engineering support for quality, manufacturing, design & development, documentation and other product-related disciplines
- Apply statistical techniques and trending to monitor products, processes and controlled work environments to identify potential corrective or preventive actions
- Specify, qualify and monitor equipment used in manufacturing processes, inspection, testing, and controlled work environments
- Perform and document investigations related to products, processes and quality systems
- Review and approve proposed change orders, deviations and nonconforming material records to determine the effect of the changes on materials, products and processes
- Conduct internal quality system audits as assigned
- Bachelor’s degree in a technical discipline, such as Engineering
- 2+ years’ experience in Quality Engineering
- Experience with Risk Management
- Experience with quality audits
- Processing and product evaluation experience and knowledge of QSR and ISO requirements
- Previous medical device industry experience
- Experience supporting high volume (500-1000 units/day) line manufacturing
- Experience with ISO 14971
- ASQ and Lean Six Sigma certifications
- Paid time off and paid volunteer time
- Medical, Dental, Vision and Flexible Spending Account
- Health Savings Account with Company Funded Contributions
- 401k Retirement Plan with Company Match
- Parental Leave and Adoption Services
- Health and Wellness Programs and Events
- Awarded 2024 Cigna Healthy Workforce Designation Gold Level
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