Sterling Industries is a leading vertically integrated contract manufacturer of medical devices. #WeManufactureSuccess
Woodbridge, Ontario
Sterling Industries is a vertically integrated contract manufacturer of medical devices and medical device components with facilities in both the US and Canada. We help companies — from Fortune 100 to mid-size to start-up — scale from launch to full production (whether it be from thousands to millions of units), with consistent and immaculate quality, process and compliance. We offer a repeatable design transfer process, design-for-manufacturing expertise, regulatory compliance and supply chain optimization. Our company mantra is: 100% on time, 100% complete and 100% quality. We manufacture success. Whether your device requires complicated machined components, intricate injection molded parts, laser cut small diameter stainless steel tubing, laser cut large format metal, robotically welded pieces, integrated electronics, ultrasonic welded parts, and/or low pressure over-molding, our team of engineers, designers and technicians can help make your product a reality. We assemble your device in a Class 7 Clean Room, a White Room or on the Shop Floor as required. We are ISO 13485:2016 Certified and 21 CFR Part 820 Compliant and are FDA and Health Canada Registered. Let’s discuss your project. Contact us by email at sales@sterlingindustries.com or call us toll-free at 1 (888) 669-0246.
Sur place · Vaughan
The Shipper/Receiver manages all shipping and receiving activities, including loading, unloading, and documenting goods in the ERP system. They are responsible for order fulfillment, courier coordination, and maintaining warehouse organization and stock accuracy.
Sur place · Vaughan
The Engineering Co-op student will support the Design Engineering team in developing and commercializing medical devices. Responsibilities include product design support, prototyping, testing, and collaboration with cross-functional teams.
Sur place · Vaughan
The Engineering Co-op student will support the Process Development Engineering team in developing and optimizing manufacturing processes for medical devices. Responsibilities include process testing, troubleshooting, validation support, and documentation.
Sur place · Vaughan
Support the Process Development Engineering team in optimizing, validating, and improving manufacturing processes for medical devices. Responsibilities include conducting validation studies, documenting work instructions, and participating in LEAN initiatives to enhance productivity.
Sur place · Vaughan
Support the Design Engineering team in developing and commercializing medical devices through 3D modeling, prototyping, and testing. Collaborate with cross-functional teams to manage engineering changes and prepare technical documentation from concept to production.