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Added 3 days ago
EO
Plant Engineer
Evonik Oxeno
Burnaby, BC
- Full-time
…process development & scale-up, analytical method development & validation to support raw material, in-process, release and stability testing, all the way through to sterile product…
Added 3 days ago
E
Plant Engineer
Evonik
Burnaby, BC
- Full-time
…process development & scale-up, analytical method development & validation to support raw material, in-process, release and stability testing, all the way through to sterile product…
Added 4 days ago
S
Validation Engineer II (Canada) (contract)
Sanofi
Toronto, ON
- Up to $60 CAD / hour
- Contract
Sanofi's contingent workforce program, FLEXT Direct, is seeking a Validation Engineer II for a 12-month contract.
Added 4 days ago
T
Data Scientist II
TD
Toronto, ON · Ottawa, ON
- Full-time
Collaborate with other partners, such as AIML scientists, data and business analysts, software engineer, data engineers, and application developers to develop scalable and sustainable…
Added 4 days ago
C
Submarine Technical Training SME-EN
CAE
Abbotsford, BC
- Full-time
You will contribute to the analysis, design, development, testing, and validation of training solutions that prepare submariners to safely and effectively operate, monitor, diagnose, and…
Added 4 days ago
C
Submarine Technical Training SME-EN
CAE
Esquimalt, BC
- Full-time
You will contribute to the analysis, design, development, testing, and validation of training solutions that prepare submariners to safely and effectively operate, monitor, diagnose, and…
Added 4 days ago
C
Submarine Technical Training SME-EN
CAE
Halifax, NS
- Full-time
You will contribute to the analysis, design, development, testing, and validation of training solutions that prepare submariners to safely and effectively operate, monitor, diagnose, and…
Added 4 days ago
C
Submarine Technical Training SME-EN
CAE
Ottawa, ON
- Full-time
You will contribute to the analysis, design, development, testing, and validation of training solutions that prepare submariners to safely and effectively operate, monitor, diagnose, and…
Added 4 days ago
C
Submarine Technical Training SME
CAE
Abbotsford, BC · Esquimalt, BC · Halifax, NS · Ottawa, ON
- Full-time
You will contribute to the analysis, design, development, testing, and validation of training solutions that prepare submariners to safely and effectively operate, monitor, diagnose, and…
Added 4 days ago
B
Aircraft Avionics Technician (CH147F)
Boeing
Calgary, AB · Vancouver, BC · Winnipeg, MB · Mississauga, ON · Ottawa, ON · Petawawa, ON · Toronto, ON · CAN - Petawawa, Canada
- Full-time
Performs validation/verification testing of systems and components.
Added 4 days ago
B
Aircraft Avionics Technician (CH147F)
Boeing
Calgary, AB · Vancouver, BC · Winnipeg, MB · Mississauga, ON · Ottawa, ON · Petawawa, ON · Toronto, ON · CAN - Petawawa, Canada
- Full-time
Performs validation/verification testing of systems and components.
Added 5 days ago
V
Design Quality Engineer II
Verathon
Burnaby, BC
- Full-time
As a Design Quality Engineer II, you will play a crucial role in supporting the quality aspects of new product development and sustaining engineering initiatives. You will work closely with…
Added 5 days ago
HA
Systems Engineer II
Honeywell Aerospace
Ottawa, ON · Kanata, ON
- Full-time
Develop verification and validation plans for complex optical systems.
Added 5 days ago
DE
Linux Systems Administrator / Engineer
Digital Extremes
London, ON
- Full-time
Digital Extremes is looking for a collaborative, driven Linux Systems Administrator to join our core IT infrastructure team onsite at our London, Ontario studio. In this role, you will work…
Added 5 days ago
Software Development Engineer II, Price Perception and Evaluation
Amazon
Vancouver, BC
The scale is rare. You will build systems that process price and order data for millions of products, every day, across Amazon's stores in more than a dozen countries. That data feeds…
Added 5 days ago
Linux Systems Administrator / Engineer
Digital Extremes
London, ON
Digital Extremes is looking for a collaborative, driven Linux Systems Administrator to join our core IT infrastructure team onsite at our London, Ontario studio. In this role, you will work…
Added 5 days ago
Senior Vehicle Systems Engineering
Geotab
Waterloo, ON
As a Senior Vehicle Systems Engineer, your key responsibilities will include leading complex vehicle investigations, reverse engineering, and root-cause analysis; defining safe and reliable…
Added 6 days ago
V
Manufacturing Engineer II
VitalBio
Oakville, ON
- Full-time
…inventory management and material supply for verification and validation…
Added 6 days ago
T®
Validation Engineer II
TekWissen ®
Markham, ON
- $45 to $47 CAD / hour
- Contract
The Client S3 Business Unit IP Systems Engineering team is seeking an energetic, dynamic, experienced IP Systems Engineer to join our growing team. We work with customers to develop new…
Added 8 days ago
R
Specialist II, Validation
Resilience
Mississauga, ON · CAN - ON - Mississauga - Meadowpine Blvd
- Full-time
The Validation Engineer II / Specialist II supports validation activities across clinical and commercial manufacturing, contributing to the regulatory compliance and quality of products…
Added 9 days ago
SI
R&D Engineer II
Stathera, Inc.
Vancouver, BC
- Full-time
The R&D Engineer is responsible for designing, analyzing, and validating board-level analog and mixed-signal circuits to support the development of high-performance electronic systems. This…
Added 9 days ago
QA Engineer II
Zafin
Ottawa, ON · Toronto, ON
…management; and Zafin IO, an integration platform that connects data, systems, and workflows across complex enterprise…
Added 10 days ago
T®
Engineering - Validation Engineer II
TekWissen ®
Markham, ON
- $47 to $49 CAD / hour
- Contract
We are looking for a dynamic, energetic Systems Test Validation Engineer to join our growing team.
Added 10 days ago
UM
Systems Engineer Senior II
Ultra Maritime
Dartmouth, NS
- Full-time
The Systems Engineer Senior II will play a leading role in a multi-disciplinary project team developing new and innovative solutions for the Royal Canadian Navy and its partners in the…
Added 12 days ago
S
Mechanical Engineer
SMARTFOX
ON · Ontario, Canada
- $75,000 to $125,000 CAD / year
- Full-time
Design and develop mechanical components, assemblies, and systems from concept through production using SolidWorks, Creo, NX, CATIA, or Inventor

VitalBio

Manufacturing Engineer II

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

The salary range for this position is $100,000 - 110,000 annually. · Full-time

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Job details

Pay: The salary range for this position is $100,000 - 110,000 annually.
Job type: Full-time
Experience: 5+ years’ significant manufacturing engineering or related operational experience in diagnostics or similar fields combining biologicals/reagents with injection-molded plastics.
Posting language: English
Posted: Oct 19, 2026

Original job description

About you:

You are a hands-on technical problem solver with deep experience in transferring products from R&D to manufacturing in a cGMP-regulated environment. You thrive where engineering, automation, and operations meet: designing, scaling, and optimizing manufacturing assembly processes that ensure quality, reliability, and efficiency. You approach each challenge with a disciplined, data-driven mindset, excel at cross-functional teamwork, and are energized by continuous improvement and innovation. You’re ready to contribute your expertise to help Vital Bio bring diagnostics to life.

What you'll do:

Lead the transfer of new products and manufacturing processes from R&D engineering and assay development into a cGMP manufacturing environment.
Design, develop, document and implement robust manufacturing processes and scale-up activities for consumable assemblies (reagents with molded plastic components) and diagnostic instruments.
Provide DFx feedback to ensure manufacturability, scalability, and cost effectiveness of new designs.
Define and evaluate different assembly strategies, identify automation opportunities, and maintain cost-effective, high-quality, repeatable operations; including Make/Buy decisions and third-party transfers.
Develop process flow maps, optimize assembly sequences applying lean principles, and recommend new processes/equipment.
Serve as the manufacturing subject matter expert, identifying risks and mitigation strategies related to process steps, raw materials, and product performance (and their interactions) throughout tech transfer.
Collaborate cross functionally with R&D engineering, assay development, manufacturing and supply chain teams to ensure effective inventory management and material supply for verification and validation needs.
Establish and maintain manufacturing controls and documentation, including SOPs, work instructions, and acceptance plans, in compliance with ISO 13485, FDA 21 CFR 820, and cGMP.
Plan and execute comprehensive validation protocols for equipment, facilities, and processes (IQ, OQ, PQ and TMV).
Perform root cause analysis for manufacturing failures with cross-functional teams and implement process improvements.

What you need:

Bachelor’s degree in a STEM discipline.
5+ years’ significant manufacturing engineering or related operational experience in diagnostics or similar fields combining biologicals/reagents with injection-molded plastics.
Proven ability to apply critical thinking, analytical reasoning, and experimental design to solve complex manufacturing problems.
Working knowledge of tech transfer, cGMP processes, process validation / /qualification (IQ/OQ/PQ/TMV), and regulated manufacturing environments.
Strong familiarity with manufacturing of reagents, consumables, and instruments for IVDs, tech transfer, cGMP processes, and validation/qualification requirements.
Experience collaborating with cross-functional teams and managing multiple projects simultaneously.
Experience with statistical process controls (SPC), design of experiments (DOE), and data analysis (Minitab, JMP, Excel).
Excellent communication skills and sharp attention to detail.
Highly organized with a proactive, solutions-oriented approach.

Bonus points for:

Six Sigma and/or Lean certification, with practical experience using these tools for process improvement.
Prior experience with high-volume automated assembly and global IVD manufacturing regulations.
Experience in scaling up manufacturing operations from pilot scale to full production mode.
Project management experience and leadership of project teams.
An appreciation for puns and a willingness to pitch in wherever needed!

The salary range for this position is $100,000 - 110,000 annually. Compensation will be determined based on the individual's demonstrated experience.

Why Join Us?

At Vital Bio, you will:

Take a critical role in building and scaling manufacturing operations for novel diagnostics, impacting global healthcare systems.
Work alongside passionate problem-solvers in a culture that values curiosity, teamwork, and innovation.
Own your contributions on projects with meaningful, real-world outcomes.
Grow your skills in a supportive, dynamic environment that believes fun and excellence go hand-in-hand.

About Vital

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

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More about this job

Responsibilities

Lead the transfer of new products and manufacturing processes from R&D into a cGMP environment while designing and optimizing assembly strategies. Collaborate with cross-functional teams to ensure quality, scalability, and compliance with regulatory standards like ISO 13485 and FDA 21 CFR 820.

Requirements

Requires a Bachelor’s degree in a STEM discipline and at least 5 years of manufacturing engineering experience in diagnostics or related fields. Candidates must possess strong knowledge of cGMP, process validation, and technical transfer within regulated manufacturing environments.

Skills

Manufacturing Engineering
Tech Transfer
cGMP
Process Validation
IQ/OQ/PQ
Root Cause Analysis
Lean Principles
Statistical Process Control
Design of Experiments
Automation
ISO 13485
FDA 21 CFR 820
Project Management
Cross-functional Collaboration
Data Analysis
Technical Problem Solving

Visa sponsorship

Not detected in the job text

Keywords

Manufacturing Engineering
cGMP
Tech Transfer
R&D
ISO 13485
FDA 21 CFR 820
IVD
Process Validation
IQ/OQ/PQ
TMV
Lean Principles
SPC
DOE
Minitab
JMP
Six Sigma
Automation
Diagnostics
Reagents
Injection-molded plastics
Root Cause Analysis
Supply Chain
Inventory Management
Scale-up
DFx
SOPs
Work Instructions
Acceptance Plans
Microfluidics
Point-of-care

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