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Boston Scientific

Process Engineering Associate, Co-op/New Grad

Mississauga, ON, Canada

Full-time

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Job details

Job type: Full-time
Apply by: Dec 3, 2026
Posting language: English
Posted: Nov 3, 2026

Original job description

Additional Locations: Canada-ON-Mississauga

Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance

At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions.

Process Engineering Associate, Co-op/New Grad

This position is a 12-month co-op/new grad/PEY placement beginning January 2027

About The Role

The Process Engineering Associate is directly involved in providing product design and manufacturability input during concept and commercialization phases as well as actively participating in continuous improvement initiatives when scaling up existing manufacturing processes.

Work mode: At Boston Scientific, we value collaboration and synergy. This role follows an on-site work model requiring employees to be in our local office at least five days per week.

Sponsorship: Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time.

Relocation: Relocation assistance is not available for this position at this time.

Your Responsibilities Will Include

Support the development and optimization of innovative manufacturing processes and equipment including generating ideas, drafting 3D prototypes in SolidWorks, coordinating testing, and researching and providing input to the team as needed.
Build and test prototype devices to ensure they meet requirements.
Assist with the development of validation and test plans by supporting engineers with the execution of process characterization and testing of devices.
Lead LEAN initiatives to make improvements to the manufacturing process.
Aid in the development and provision of technical documentation by preparing drawings, writing work instructions, and providing training for new tools and equipment.
Design test methods or follow standard protocols to ensure the device meets the patients’ needs.
Monitoring safety practices and ensuring ISO 13485 and FDA compliance while collaborating with cross functional teams to meet product timelines.
In all actions, demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures.
Other duties as required.

Required Qualifications

Actively enrolled in an Engineering degree, or a recent graduate from a Bachelor's degree in Engineering

Preferred Qualifications

Six Sigma or LEAN knowledge
Experience with SolidWorks and Minitab
Experience in a highly regulated manufacturing environment
Strong interest in biomedical technology
Motivated self-starter with a hands-on approach
Ability to work independently and with a diverse group of Engineers and Clinicians
Excellent communication skills, both written and oral
Strong leadership and problem-solving skills
Positive attitude and enthusiasm

Requisition ID: 635662

Minimum Salary: $[[cust_salaryMin]]

Maximum Salary: $[[cust_salaryMax]]

The anticipated compensation and the value of core and optional employee benefits offered by Boston Scientific (BSC) – see www.bscbenefitsconnect.com--will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role. Compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, among other relevant business or organizational needs.

Compensation for hourly, non-sales roles may also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements).

Compensation for salaried, non-sales roles may also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).

Compensation for sales roles is governed by Sales Incentive Compensation Plan (which includes certain annual non-discretionary incentives based on predetermined objectives).

Boston Scientific transforms lives through innovative medical technologies that improve the health of patients around the world. As a global medical technology leader for more than 45 years, we advance science for life by providing a broad range of high-performance solutions that address unmet patient needs and reduce the cost of healthcare. Our portfolio of devices and therapies helps physicians diagnose and treat complex cardiovascular, respiratory, digestive, oncological, neurological and urological diseases and conditions. Learn more at www.bostonscientific.com and follow us on LinkedIn.

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More about this job

Responsibilities

Support the development, optimization, testing, and validation of medical-device manufacturing processes and equipment, including building prototypes and contributing to process improvements. Prepare technical documentation and training, design or follow test methods, and collaborate with cross-functional teams while maintaining patient safety, product quality, and regulatory compliance.

Requirements

Applicants must be actively enrolled in an engineering degree program or be recent graduates with a bachelor's degree in engineering. Preferred qualifications include Lean or Six Sigma knowledge, experience with SolidWorks and Minitab, regulated manufacturing experience, interest in biomedical technology, and strong communication, leadership, and problem-solving skills.

Skills

Manufacturing Process Development
Process Optimization
SolidWorks
Minitab
Prototype Development
Process Characterization
Validation Testing
Lean Manufacturing
Technical Documentation
Test Method Design
ISO 13485 Compliance
FDA Compliance
Cross-Functional Collaboration
Problem-Solving
Communication
Leadership

Visa sponsorship

Not detected in the job text

Keywords

Process Engineering
Medical Device Manufacturing
Manufacturing Process Development
Process Optimization
SolidWorks
Minitab
3D Prototyping
Prototype Devices
Process Characterization
Validation Plans
Device Testing
Lean
Six Sigma
Continuous Improvement
Technical Documentation
Work Instructions
Test Method Design
ISO 13485
FDA Compliance
Quality Policy
Patient Safety
Product Quality
Biomedical Technology
Regulated Manufacturing
Cross-Functional Collaboration

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