About this opportunity
Laborie Medical Technologies Corp lists this Quality Engineer II opportunity in murray, Utah. Review the employer’s description below for duties, qualifications and application requirements.
Job description
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:
The Quality Engineer II ensures product and process conformity to requirements. Ensuring documentation in conformance to the Quality Management Systems and applicable standards and regulations.
About the Role:
Establish and maintain documentation for the inspection and release of raw materials, sub-assemblies and finished medical devices
Perform quality activities in support of Operations, contractmanufacturersand R&D
Schedule and document calibration and maintenance activities
Support design and engineering change processes and associated documentation
Support internal and external audit activities and work to resolve audit nonconformities.
Perform and support process, equipment validations.
Investigate,dispositionand close nonconformities.
Investigate and close product complaints.
Collect and evaluate quality data for process monitoring, managementreviewand post market surveillance
Perform quality activities related to CAPA processes
Represent Quality Engineering in the development and maintenance of process and product risk assessments (e.g.pFMEAsdFMEA)
Participate in Material Review Board reviews including material segregation, investigation,correctionsand dispositions
Minimum Qualifications:
At least 5 years Medical Device quality engineering experience
B.S. in engineering or science
Strong knowledge of FDA QSR and ISO 13485 requirements
Critical thinking and sound decision-making skills
Excellent written and verbal communication skills
Ability to independently solve problems, leadprojectsand influence teams
Demonstrated ability to work as a team player with multi-disciplinary project teams
Demonstrated ability to interpret technical information
Experience with quality audits (lead auditor certification preferred)
ASQ certification preferred
Lean Six Sigma training preferred
Why Laborie:
Our Mission every day is to operate as a world-class specialist medical company making and advancing technologies that preserve and restore human dignity. We do that today by helping people with pelvic and gastrointestinal conditions live normal lives, and by helping mothers and babies have safe deliveries.
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
Laborie provides equal employment opportunities and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. Laborie is committed to providing access and reasonable accommodation in our services, activities, education, and employment for individuals with disabilities.
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Who can apply
Review the original listing for work authorization, qualifications and employer requirements.