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Advanced Quality Technician

Stryker

This is a Full-time position in Portage, MI posted September 9, 2021.

About Stryker
Stryker is one of the worlds leading medical technology companies and, together with our customers, is driven to make healthcare better.

We offer innovative products and services in Orthopaedics, Medical and Surgical, and Neurotechnology and Spine that help improve patient and hospital outcomes.

We are proud to be named one of the Worlds Best Workplaces and a Best Workplace for Diversity by Fortune Magazine.

Learn more about our award-winning organization by visiting
Come join our team of talented engineers and help us develop innovative products to help our customers!
Who we are: Stryker is one of the worlds leading medical technology companies and is dedicated to helping healthcare professionals perform their jobs more efficiently while enhancing patient care.

The Company offers a diverse array of innovative medical technologies, including reconstructive, medical and surgical, and neurotechnology and spine products to help people lead more active and more satisfying lives.
We are currently seeking an Advanced Quality Technician in Portage, MI.
Who we want:
Detail-oriented process improvers.

Critical thinkers who naturally see opportunities to develop and optimize work processes finding ways to simplify, standardize and automate.
Collaborative partners.

People who build and leverage cross-functional relationships to bring together ideas, data and insights to drive continuous improvement in functions.
Dedicated achievers.

People who thrive in a fast-paced environment and will stop at nothing to ensure a project is complete and meets regulations and expectations.
What you will do:
Collaborate with cross-functional teams to develop inspection methods to be used internally and at Suppliers.
Track PPAP progress and drive timely completion of component qualification which includes close collaboration with vendors and cross-functional team members.
Manage non-conformances on interim approval PPAPs and identify a plan for closure.
Coordinate component measurement efforts whether executed internally or externally.
Support Production Part Approval Process (PPAP) activities.
Collaborate with cross-functional teams to initiate PPAP planning for initial release engineering drawings.
Provide metrology support services to Suppliers and internal customers.

Partner with suppliers as needed execute deliverables for component qualification (process flow, certificate of compliance, REACH/RoHS, and general evidence/paperwork requirements).
Provide MRB support during the new product development process and up to 1 year after product launch.
Engage in design and development activities, including quality transfer to operations quality
What you will need:
Basic Qualifications:
High school education or equivalent.
2 years of experience in quality, manufacturing or service fields
Preferred Qualifications:
Experience working in a regulated industry such as medical device, automotive, aerospace or electronics
Working mechanical aptitude
Ability to operate small hand tools (e.g., pliers, screwdrivers, hammer, wrenches, etc.) and small power tools
Working knowledge of common hand gages (calipers, micrometers, pin gage, etc.)
Working understanding of engineering drawings
Working knowledge of Manufacturing, Fabrication, and Assembly
Working Knowledge GD&T
Working knowledge of quality system regulations.
Basic understanding of CAD models and CAD software.

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