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TITLE: Quality Engineering UNIPOINT OCCUPATION ID: QUAL ENG REVISION: Rev 01 DEPARTMENT: Quality POSITION OBJECTIVE: Responsible for the launch and daily management of the processes, products, equipment, people and custo…
Skills: Quality Management Systems, Root Cause Analysis, Corrective Actions, CMM Programming, SPC Systems
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Process Engineering - Co-op Student Sterling Industries – Whitmore, ON Co-op Term: Fall 2026 / Winter 2027 (8-month) About the Company Sterling Industries is a fast-growing North American based contract manufacture…
Skills: Process Development, Validation (IQ/OQ/PQ), Lean Manufacturing, Root Cause Analysis, SolidWorks
Vaughan, Ontario, Canada · On-site
$20/hr–$22/hr
Design Engineering - Co-op Student Sterling Industries – Whitmore, ON Job Type: Co-op About the Company Sterling Industries is a fast-growing North American based contract manufacturer and assembler of medical devi…
Skills: SolidWorks, 3D Modeling, Prototyping, Design For Manufacturability, Design For Assembly
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Responsible for the launch and daily management of quality processes, products, and equipment to ensure regulatory compliance. This includes performing root cause analysis, managing non-conformances, and overseeing gage calibrations and CMM programming.
Requires a bachelor's degree in engineering and 5-8 years of quality experience within an ISO registered environment. Proficiency in problem-solving methods like 8D and Fishbone, as well as Six Sigma certification, is highly preferred.
TITLE: Quality Engineering
UNIPOINT OCCUPATION ID: QUAL ENG REVISION: Rev 01
DEPARTMENT: Quality
POSITION OBJECTIVE: Responsible for the launch and daily management of the processes, products, equipment, people and customers in regards to the quality management system and regulatory requirements.
DIRECT REPORTS: None
1. Development and implementation of all quality related processes and documentation for new program development and current sustainment business.
2. Direct involvement in manufacturing process development and continuous improvement as to meet or exceed the company’s quality metrics and process metrics for current and new business.
3. Review, analysis, and resolution of customer/internal/supplier quality issues through root cause analysis and implementation of corrective actions.
4. Development and implementation of preventative actions and continuous improvements within the manufacturing and quality areas.
5. Control of the non-conformance area (inventory, disposition, and associated costs)
6. Purchase, management and review of gage equipment, certifications and calibrations. Including programing CMM or other coordinate measurement equipment.
7. Ensure the Gage calibration log is complete and up to date.
8. Coordinate with the quality inspector for the daily inspection, measurement, test, and approval of all components, product, process and use of quality metrics to ensure quality targets are met.
9. Communicate and coordinate with management, administrative, operations, quality, and engineering departments.
10. Daily use of quality management system software and SPC systems.
JD –QUAL ENG
Rev. 01
Pg. 2 of 3
Job Description
11. Participate in conducting supplier and internal system and process audits.
12. Additional duties as requested by management.
WORKING RELATIONSHIPS: Operations department, Quality department, customers, suppliers
1. Engineering bachelor’s degree, with technical and mathematical focus preferred.
2. 5-8 years of experience in a quality department in an ISO registered environment
3. High volume workload requires conscientious attitude with accuracy and attention to detail.
4. Knowledge and experience on:
a. ISO 9001 (ISO 13485 a plus)
b. Process capability and effect on processes, production, equipment, and assembly)
c. Problem solving methods (5Y, Fishbone, 8D, etc.).
d. Ability to be self-managed and directed from a satellite operation
5. Six Sigma certifications a plus (green belt of higher)
6. Proficient in with Microsoft office (outlook, excel, word, power point)
7. Good communication skills (oral, written, technical)
8. Excellent time management skills and the ability to be self-directed
9. Customer focus and continuous improvement approach.
10. Experience with machining, fabrication, and assembly operations a plus
11. Must be able to work a flexible schedule and lift minimum 40 pounds.
12. The position will require some travel (USA and Canada).
REPORTS TO: Quality Manager
Sterling Industries is a leading vertically integrated contract manufacturer of medical devices. #WeManufactureSuccess
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 [email protected] or call us toll-free at 1 (888) 669-0246.
Offices: 10 Whitmore Rd, Woodbridge, Ontario L4L 7Z4, CA · 295 Connie Crescent, Vaughan, Ontario L4K 5R2, CA · 6825 Beatrice Drive, Kalamazoo, MI 49009, US · 72 Churchill Drive, Unit 5, Barrie, Ontario L4N 8Z5, CA
Sterling Industries is a leading vertically integrated contract manufacturer of medical devices. #WeManufactureSuccess
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 [email protected] or call us toll-free at 1 (888) 669-0246.
Offices: 10 Whitmore Rd, Woodbridge, Ontario L4L 7Z4, CA · 295 Connie Crescent, Vaughan, Ontario L4K 5R2, CA · 6825 Beatrice Drive, Kalamazoo, MI 49009, US · 72 Churchill Drive, Unit 5, Barrie, Ontario L4N 8Z5, CA
