Engineering - Co-op Student - Process Engineering

Sterling Industries; Vaughan; On-site; CAD 40,000 - 60,000; Full time

Job summary

Sterling Industries in Vaughan is seeking an Engineering Co-op student for Fall 2026 / Winter 2027. This role focuses on supporting the Process Development Engineering team in optimizing and validating manufacturing processes for medical devices.

The ideal candidate will be enrolled in a relevant engineering degree program and have a strong interest in medical device development. Key responsibilities include assisting in process documentation, participating in continuous improvement initiatives, and supporting trial runs in a regulated environment.

Qualifications

• Currently enrolled in a relevant Bachelor's program.
• Strong interest in medical device product development.
• Hands-on and self-motivated with problem-solving skills.
• Excellent verbal and written communication skills.
• Ability to work independently and collaboratively.

Responsibilities

• Support development and optimization of manufacturing processes.
• Assist with process characterization and validation studies.
• Participate in LEAN and continuous improvement initiatives.
• Support trial runs and manufacturing transfer activities.
• Collect, analyze, and summarize engineering data.

Skills

Learning Agility

Analytical Thinking

Attention to Detail

Initiative

Team Collaboration

Education

Bachelor’s degree in Mechanical, Industrial, Biomedical Engineering, or related discipline

Tools

SolidWorks

CAD software

Job description

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.