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Added 24 mins ago
E
Journeyman PLT for EPCOR System Repair Services
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- Full-time
We are hiring two (2) full time, permanent Power Line Technician (PLT) positions working out of Edmonton Alberta.
Added 24 mins ago
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Added 1 hour ago
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Added 1 hour ago
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Technicien(ne) en amélioration continue de qualité / Quality Continuous Improvement (QCI) Tech - French
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Added 1 hour ago
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Added 1 hour ago
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Added 1 hour ago
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Field Technician
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Added 1 hour ago
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VitalBio

Manufacturing Technician I

400 Iroquois Shore Rd, Oakville, ON, L6H 1M5, Canada

The compensation range for this role is $20.00-$24.50 / hour. · Full-time

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Job details

Pay: The compensation range for this role is $20.00-$24.50 / hour.
Job type: Full-time
Experience: 3+ years of industry experience in medical device or electronic assembly, preferably in a cGMP environment;
Posting language: English
Posted: Oct 26, 2026

Original job description

About you:

In this technical production role, you will be responsible for the manufacture and assembly of consumable components for the Vital Bio medical diagnostic platform from raw materials through to the final packaged product. The primary focus of the role will be with the ongoing scale-up of the manufacturing process. As a member of the Manufacturing team you will be an integral part of Vital Bio’s efforts to launch commercial production of the company’s innovative medical diagnostic technology.

Working directly with all supporting functions, this role will apply well defined processes through work instructions, batch production records, manufacturing aids to generate products intended for commercial distribution.

What You’ll Do:

Setup, prepare, and execute processes with high quality and consistency which generate products meeting specifications as intended for commercial use, including:
- Build of consumable assemblies
- Dispense of liquid formulations
- Lyophilization, bead sieving and sorting
- Disc assembly
- Packaging

Generate and complete all associated documentation using current Good Documentation Practices (GDP) including Batch Production Records;
Maintain accurate records of production, including taking inventory of production and prototype materials through cycle counting and physical inventories;
Set up, operate, and monitor automated and semi-automated equipment used in the assembly process;
Collaborate in the development, setup, and maintenance of cGMP processes at production scale;
Provide feedback and recommendations to the manufacturing engineering team for improvements to manufacturing work instructions, assembly, and test fixtures and processes
Provide feedback and recommendations to supervisors and JH&S Committee regarding Health & Safety concerns/near-misses/incidents;
Apply 5S and lean principles to maintain organization and good housekeeping practices in the manufacturing area;
Work with associated development and engineering teams to incorporate improvements into the manufacturing process based on testing results and observations;
Participate in process FMEAs and risk identification as well as assisting with the implementation of appropriate countermeasures;
Assist Manufacturing Engineering in the setup and validation of new equipment for use in the assembly process;
Execute daily, weekly, and monthly preventive maintenance and cleaning activities of equipment and manufacturing areas;
Support and participate in root cause investigations for, Out-of-Specification (OOS) investigations, Quality Incident Notifications, and CAPA actions related to manufactured products and manufacturing processes;
Maintain a high level of work-related training to ensure consistency of performance, including cross-training on multiple processes within Manufacturing;

What You’ll Need:

High school diploma or higher;
3+ years of industry experience in medical device or electronic assembly, preferably in a cGMP environment;
Very good manual dexterity and visual acuity;
Ability to read and understand written assembly and test instructions;
Demonstrated strong organizational skills in your day-to-day performance and ability to multitask across projects and activities;
Excellent communication skills and attention to detail;
Proven ability to collaborate cross-functionally and participate in multi-disciplinary teams.

Bonus points for:

Experience with reagent preparation, operation of (semi-)automated manufacturing systems
Experience with 5S, kanbans, and lean manufacturing processes;
Prior experience with single-use assemblies, reagent fill and seal, and lyophilization processes;
An appreciation of puns!

Why Join Us?

At Vital Bio, you will:

Get an opportunity to shape the future of medical diagnostics and make a meaningful impact on global healthcare;
Be in collaborative environment with a high-performing team dedicated to innovation and excellence;
Have a platform to showcase your talents and grow professionally in a company that values your contributions.

The compensation range for this role is $20.00-$24.50 / hour. Compensation will be determined based on the individual’s demonstrated experience, education, training, relevant certifications or licensure, and other applicable business and organizational factors.

This role is a current, onsite vacancy.

About Vital Bio

Vital is revolutionizing point-of-care diagnostics with our VitalOne platform, delivering real-time care wherever patients are. Our mission is to democratize health technology, making healthcare more accessible and proactive.

Our global team of experts spans chemistry, software, engineering, and microfluidics. We thrive on change, operate on trust, and value diverse perspectives. Our growth-minded culture empowers front-line decision-making and fosters impactful work.

We seek tenacious, bold individuals ready to transform healthcare. At Vital, your talent will make a difference as we work to ensure everyone has access to care when and where they need it.

Vital Biosciences Inc. is an equal opportunity employer and values diversity in the workplace. We are therefore happy to accommodate any individual needs in keeping with the Ontario Human Rights Code and the Accessibility for Ontarians with Disabilities Act. If you require accommodation in order to participate in our hiring process, please contact us to make your needs known in advance

As part of our recruitment process, we may use automated or AI-supported tools to assist with application review and screening. These tools are used to support, not replace, human decision-making. Final hiring decisions are always made by our hiring team.

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More about this job

Responsibilities

Manufacture and assemble diagnostic consumables from raw materials through packaging, following production instructions and quality requirements for commercial use. Maintain production records and inventory, operate and maintain equipment, support process scale-up and improvement, and participate in risk, quality, and safety activities.

Requirements

Requires a high school diploma or higher and at least three years of industry experience in medical device or electronic assembly, preferably in a cGMP environment. Candidates should have strong manual dexterity, visual acuity, organizational and communication skills, attention to detail, and the ability to follow instructions and collaborate across teams.

Skills

Medical Device Assembly
Manufacturing Process Execution
Liquid Formulation Dispensing
Lyophilization
Packaging
Good Documentation Practices
cGMP
Automated Equipment Operation
Inventory Management
Preventive Maintenance
Root Cause Investigation
CAPA
Process FMEA
5S
Lean Manufacturing
Cross-Functional Collaboration

Visa sponsorship

Not detected in the job text

Keywords

Medical Diagnostics
Medical Device Manufacturing
Consumable Assemblies
Reagent Preparation
Liquid Formulations
Lyophilization
Bead Sieving
Disc Assembly
Packaging
Good Documentation Practices
Batch Production Records
cGMP
Automated Manufacturing Systems
Semi-Automated Equipment
5S
Kanban
Lean Manufacturing
Process FMEA
Risk Identification
Preventive Maintenance
Root Cause Investigation
Out-of-Specification Investigations
Quality Incident Notifications
CAPA
Cycle Counting
Equipment Validation
Health and Safety
Cross-Functional Collaboration

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