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Added 1 min ago
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Added 16 mins ago
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Sr. Developer - Application Development JAVA N 4B
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Senior Manager-Design Engineering
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Senior Manager, Country Quality (Canada)
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Added 1 hour ago
HR
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Baylis Medical Technologies

Process Engineering Associate

ON, Canada
Mississauga, ON, L4W 5S4, Canada

Full-time

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Job details

Job type: Full-time
Posting language: English
Posted: Oct 8, 2026

Original job description

A peek into your purpose

In our Process Engineering Department, our Engineers focus on the design, development and optimization of cutting-edge manufacturing processes and technologies to produce high-tech devices used in medical procedures. Our Process Engineers are directly involved with 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.

Role commitments

You will 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
You will work on equipment to improve the manufacturing process. This includes; the design and development of new tools and fixtures, automating simple motions or changes to improve existing equipment
You will build and test prototype devices to ensure they meet requirements
You will assist with the development of validation and test plans by supporting Engineers with the execution of process characterization and testing of devices
You will take on LEAN initiatives to make improvements to the manufacturing process
You will aid in the development and provision of technical documentation by preparing drawings, writing work instructions, and providing training for new tools and equipment
You will participate in testing of manufacturing processes and equipment. You will design test methods or follow standard protocols to ensure the device meets the patients needs
You will be responsible for monitoring safety practices and ensuring ISO 13485 and FDA compliance while collaborating with cross functional teams to meet product timelines

What we expect

Actively working towards a Degree in Engineering; Do not apply if you are not currently enrolled in the 2026/2027 school year
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

Stand-out skills

Six Sigma or LEAN knowledge
Experience with SolidWorks and Minitab
Experience in a highly regulated manufacturing environment

Perks with purpose

Effortless commute: say goodbye to commuting challenges/hassles with our complimentary shuttles and subsidized transit options, making your journey to work a breeze.
Work-life integration: Embrace a well-balanced work-life rhythm through our hybrid model and flexible hours, empowering you to thrive both personally and professionally.
Nurturing your career: Propel your career forward with abundant opportunities for on-site training, workshops, and personal development.
Unleash your spirit: Join a thriving workplace culture filled with employee-led clubs, campaigns, sports teams, and exhilarating activities – fostering camaraderie and fun.

Our MedTech Legacy

Baylis Medical Technologies is a leader in the development and manufacturing of innovative medical devices in the fields of radiology and cardiology. Headquartered in Canada, the company also provides contract manufacturing services to some of the world's leading medical device companies.

Baylis Medical Technologies is an equal opportunity employer. We are committed to providing a diverse and inclusive work environment, while providing ongoing education for all employees. Qualified applicants will be considered without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status. We firmly believe that our differences make us stronger.

Please inform us if you require any accommodation during the recruitment process.

Ready to Innovate? Apply now!

Want to experience the dynamic world of medical device innovation and be part of our visionary team at Baylis? Apply today and join our tight-knit community of innovators.

Let your passion for innovation shine at Baylis!

While we thank all applicants, only those being considered for an interview will be contacted.

Interested in learning more about careers and life at Baylis? See all our current job opportunities here and follow us on LinkedIn!

Get an exclusive peek into the world of Baylis and the incredible work we do to reshape the future of MedTech.

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More about this job

Responsibilities

The Process Engineering Associate will support the design, development, and optimization of manufacturing processes for medical devices. Responsibilities include creating 3D prototypes, conducting testing, ensuring regulatory compliance, and implementing LEAN initiatives.

Requirements

Candidates must be currently enrolled in an engineering degree program for the 2026/2027 school year. Strong interest in biomedical technology, hands-on experience, and proficiency in tools like SolidWorks are highly desired.

Skills

Process engineering
SolidWorks
Minitab
LEAN
Six Sigma
Manufacturing process optimization
Technical documentation
Validation and test planning
ISO 13485 compliance
FDA compliance
3D prototyping
Problem-solving
Leadership
Communication
Biomedical technology

Benefits

Complimentary shuttles
Subsidized transit options
Hybrid work model
Flexible hours
On-site training
Workshops
Personal development
Employee-led clubs
Sports teams

Visa sponsorship

Not detected in the job text

Keywords

Process Engineering
Manufacturing
Medical Devices
SolidWorks
Minitab
LEAN
Six Sigma
ISO 13485
FDA
Prototyping
Validation
Biomedical Technology
Radiology
Cardiology
Continuous Improvement
Technical Documentation
Automation
Cross-functional Collaboration
Quality Assurance
Engineering

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