Manufacturing Engineer I

VITALBIO; Oakville; On-site; CAD 114,000 - 135,000; Full time

Job summary

Vital Bio is seeking a hands-on Manufacturing/Process Transfer Engineer to move new products from development into scalable cGMP manufacturing. You will design processes, perform design transfer, and partner with Engineering and Quality to ensure robust, high-quality production of diagnostic assemblies.

You will lead risk assessments, implement process controls, and drive continuous improvement from prototype through full-scale production, ensuring compliance and timely execution.

Qualifications

• Bachelor’s degree in STEM is required.
• 5+ years of manufacturing engineering/operational experience in Diagnostics or similar.
• Demonstrated critical thinking and analytical reasoning.
• Ability to apply disciplined engineering approach to design experiments and analyze data.
• Familiarity with manufacturing of reagents, consumables, and instruments for IVDs; cGMP experience.
• Excellent communication and attention to detail.
• Strong organizational skills; ability to multitask and work cross-functionally.

Responsibilities

• Transfer manufacturing processes into a cGMP environment.
• Design and conduct process development activities and provide tech transfer inputs.
• Identify risks and develop mitigations for scale-up.
• Interface with Engineering to define manufacturing and inventory control processes.
• Support prototype consumables manufacturing for assay design verification and validation.
• Establish manufacturing processes and controls from prototype to production scale-up.
• Develop and improve cGMP manufacturing processes and operations.
• Lead validation activities for equipment, facilities, and processes.
• Identify, install, qualify, and maintain critical manufacturing equipment.
• Create and maintain cGMP documentation and SOPs for ISO13485 and cGMP.

Skills

Manufacturing engineering experience

Critical thinking

Disciplined engineering approach

Familiarity with IVD manufacturing

Excellent communication

Strong organizational skills

Cross-functional collaboration

Education

Bachelor’s degree in STEM

Tools

IQ/OQ/PQ

Job description

About you:

In this Technical role, you will be responsible for the transfer of new products from engineering and assay development into manufacturing, designing, and developing assembly processes that assure the consistent and cost-effective production of high-quality, repeatable assemblies in prototypes through manufacturing scale-up and steady-state production in a cGMP environment. This will include investigating and assessing different assembly processes, developing, implementing, and maintaining processes and automated equipment for the prototyping, scale-up and production of sub-assemblies, and final assemblies incorporating reagents with molded plastic components. Developing process flow maps and optimal assembly sequences, based on the application of lean principles, as well as investigating, evaluating, and recommending new processes and equipment, Make/Buy recommendations, and transferring to third-party vendors as appropriate.

What you'll do:

• Execute the transfer of manufacturing processes and technologies from Research and Process Development groups into a cGMP environment;

• Design the appropriate manufacturing processes, define and conduct process development activities and provide design transfer inputs required as part of Tech Transfer;

• As the manufacturing Subject Matter Expert, identify potential risks, evaluate impacts of manufacturing process steps and raw materials on product performance, and develop risk mitigations as part of the tech transfer and scale-up;

• Interface with Engineering teams to define and establish manufacturing and inventory control processes for reagents, consumables, and instruments;

• Support the Assay Development and Engineering teams to ensure the manufacture and supply of prototype consumable assemblies needed for assay design verification and clinical validation activities;

• Establish appropriate manufacturing processes and controls to create and maintain consistency and quality of manufacturing from prototype through production scale-up;

• Utilize your knowledge and experience to develop, assess, implement, and continually enhance cGMP manufacturing processes and operations;

• Lead comprehensive validation activities including planning and execution of validation protocols for equipment, facilities, and processes;

• Identification, procurement, installation, qualification (IQ, OQ, PQ), and maintenance of critical manufacturing equipment;

• Create and maintain cGMP manufacturing documentation (e.g. Work Instructions, in-process, and final acceptance plans and records);

• Support the creation and maintenance of Standard Operating Procedures (SOPs) for ISO13485 and cGMP processes;

• Perform Root Cause Analysis of manufacturing failures, in collaboration with cross-functional team members, to determine failure causes, and define and implement improvements to address the causes of failures;

• Drive Continuous Improvement in manufacturing by identifying improvement opportunities and developing and implementing process improvements.

What you need:

• Bachelor’s degree in STEM;

• 5+ years of significant manufacturing engineering and/or operational experience in Diagnostics or similar industries combining biologicals and reagents with injection molded components;

• Demonstrated critical thinking and analytical reasoning skills;

• Ability to apply a disciplined engineering approach to define and execute designed experiments, analyze data as well as define problems, collect data, establish facts, and draw valid conclusions;

• Familiarity with the manufacturing of reagents, consumables, and instruments for IVDs, validation/qualification requirements, and cGMP processes;

• Excellent communication skills and attention to detail;

• Strong organizational skills and ability to multitask across projects and activities;

• Proven ability to collaborate and work effectively with cross-functional teams.

Bonus points for:

• Six Sigma and/or Lean certification with demonstrated experience in applying the tools and methodologies to real-life practical situations;

• Familiarity with global IVD regulations related to manufacturing;

• Prior experience with high-volume automated assembly processes;

• Experience with Project Management and leading project teams;

• An appreciation of puns!

Why Join Us?

At Vital Bio, you will:

• Play a key role in keeping our labs and production lines supplied with the right materials at the right time.

• You’ll see a direct connection between your work and our ability to build, test, and ship diagnostic products that impact patient care.

• You’ll collaborate closely with Supply Chain, Inventory, Manufacturing, and Quality in a fast-paced, mission-driven environment.

• As we scale, you’ll have the opportunity to refine shipping and receiving processes, contribute to new workflows, and grow your skills alongside a team that values clarity, ownership, and thoughtful execution.

The salary range for this position is $80,000 - 95,000 annually. Compensation will be determined based on the individual's demonstrated experience.

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.