INTERNSHIP DETAILS

Engineering - Co-op Student - Process Engineering

CompanyJ Sterling Industries
LocationVaughan
Work ModeOn Site
PostedJune 9, 2026
Internship Information
Core Responsibilities
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.
Internship Type
intern
Salary Range
CA$20 - CA$22
Company Size
100
Visa Sponsorship
No
Language
English
Working Hours
40 hours
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About The Company
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.
About the Role

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 manufacturer and assembler of medical devices and sub-components. We help clients deliver successful products by providing scaled production, design-for-manufacturing expertise, supplier consolidation and other critical value chain services.

Position Objective

The Engineering Co-op student will support the Process Development Engineering team in the development, optimization, validation, and continuous improvement of manufacturing processes for medical devices. The role includes process testing, troubleshooting, validation support, documentation, and manufacturing improvement initiative. 

MAJOR DUTIES:

  • Support the development and optimization of manufacturing processes, tooling, fixtures, and equipment
  • Assist engineers with process characterization, DOE activities, validation studies (IQ/OQ/PQ), and process troubleshooting
  • Participate in LEAN and continuous improvement initiatives to improve quality, efficiency, and productivity
  • Assist with process documentation including work instructions, process flows, validation reports, and training materials
  • Support trial runs, pilot builds, and manufacturing transfer activities
  • Collect, analyze, and summarize engineering and production data
  • Support root cause investigations and corrective actions
  • Cycle time studies and assembly line balancing
  • Monitor and support compliance to ISO 13485, FDA, and internal quality requirements

FUNCTIONAL COMPETENCIES

  • Learning Agility - Demonstrates curiosity and quickly learns manufacturing processes and systems. 
  • Analytical Thinking - Uses basic date analysis to support troubleshooting and process improvements. 
  • Attention to Detail - Ensures accuracy in documentation and adherence to procedures.
  • Initiative - Proactively supports production needs and seeks opportunities for improvement. 
  • Team Collaboration - Works effectively with cross-functional teams in a production environment. 

POSITION REQUIREMENTS

  • Currently enrolled in a Bachelor's degree program in Mechanical, Industrial, Biomedical Engineering, or related discipline
  • Strong interest in medical device product development and design
  • Hands-on and self-motivated with strong problem-solving abilities
  • Excellent verbal and written communication skills
  • Ability to work independently and collaboratively within cross-functional teams 
  • Experience with SolidWorks or other CAD software is preferred
  • 3D printing experience is an asset
  • Knowledge of engineering drawings and prototyping is an asset
  • Experience in a manufacturing or regulated environment is considered an asset

We will review applications as they are received. Qualified applicants will be contacted. 

Key Skills
Process DevelopmentValidation (IQ/OQ/PQ)Lean ManufacturingRoot Cause AnalysisSolidWorksCAD Software3D PrintingData AnalysisProcess CharacterizationDOE ActivitiesTechnical DocumentationCycle Time StudiesLine BalancingISO 13485 CompliancePrototypingProblem Solving
Categories
EngineeringManufacturingHealthcareScience & Research