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Manager, Product Manufacturing
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- Full-time
We are looking for an engineer with deep manufacturing process knowledge and strong project and people leadership to lead new product manufacturing at Inertia. You will take products from…

Inertia

Manager, Product Manufacturing

Toronto, ON, M3B 1T1, Canada

Hybrid

Full-time

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Job details

Job type: Full-time
Workplace: Hybrid
Experience: 10+ years of progressive experience in the production of complex electromechanical products, including 4+ years in an ISO 13485, FDA-regulated, or equivalent quality environment.
Posting language: English
Posted: Oct 28, 2026

Original job description

Manager, Product Manufacturing

We are looking for an engineer with deep manufacturing process knowledge and strong project and people leadership to lead new product manufacturing at Inertia. You will take products from engineering release through design transfer, process validation, pilot build, and production, working across our ISO 13485 and ISO 9001 facilities in Toronto and our sister manufacturing entity in Guangzhou. Much of this work is in medical devices and diagnostics, where manufacturing readiness and quality records are part of the product, with the balance in cleantech and industrial hardware.

In this role you will lead complex, high-value manufacturing programs, work directly with clients and suppliers, own the quality plan for each program, and help evolve the practices and systems that let Inertia carry products through to launch and scale.

About Inertia

Inertia Group is a Toronto-based product strategy, engineering, and manufacturing company. We help scaling hardware companies, regulated product manufacturers, and OEMs turn complex product challenges into manufacturable, launch-ready outcomes. Our work is concentrated in medical devices, diagnostics, cleantech, and industrial hardware, where technical depth, regulatory rigor, and manufacturing readiness decide whether a product succeeds.

Unlike firms that stop at design or hand off at the factory door, Inertia carries products through the full journey: validating demand, engineering with discipline, and building manufacturability and quality in from the start. We operate ISO 13485 and ISO 9001 certified facilities in Toronto, with manufacturing capability extending through our sister entity in Guangzhou.

Our clients range from funded startups to multinationals. What they share is a hard product problem and the need for a partner who takes real ownership of the outcome. For the people on our team, that means working across the whole product journey rather than one slice of it, and seeing the things you build reach production and the people who use them. See examples of our work at www.inertiapd.com.

Key Responsibilities

As Manager, Product Manufacturing, reporting to the VP Manufacturing, you will:

Manufacturing readiness and design transfer

Lead manufacturing programs from engineering release through design transfer, pilot build, process validation, and production, so that products reach manufacturing validated, documented, and supportable.
Build and own the quality plan for each program, scaled to its quality tier, including DMR and DHR structure, pFMEAs, control plans, inspection plans, and work instructions.
Plan and execute process validation (IQ, OQ, PQ) and production part approval with the engineering and quality teams.
Drive DFM and DFA reviews, make-versus-buy decisions, and cost modeling during engineering, so manufacturability and cost are built in rather than discovered at the factory.

Programs, clients, and suppliers

Manage scope, budget, schedule, quality, and risk for complex manufacturing programs with a combined value of $1M to $2M per year, and keep clients informed through clear, frequent communication.
Qualify, manage, and audit suppliers and contract manufacturers in Canada and offshore, including supplier controls under ISO 13485.
Coordinate production planning, builds, and sustainment across Toronto and our sister entity in Guangzhou, including travel to our Guangzhou facility and to suppliers.
Manage manufacturing change control, nonconformance, and CAPA for the programs you lead, and support client and regulatory audits.
Own quality tier assignment at proposal stage, and contribute manufacturing scope, cost, and schedule estimates to proposals.

People leadership

Lead and develop a team of engineers, technicians, and logistics staff; set clear expectations, manage performance, and coach each person toward their own goals and Inertia’s.
Build a team environment that is supportive, demanding, and open, where people raise risks early and ask for help before problems compound.
Develop strong working relationships across disciplines, functions, and the Toronto and Guangzhou teams.

Practices and systems

Use and strengthen Inertia’s Quality Management System and project management practices, and lead continuous improvement in how we take products to production.
Actively support workplace health, safety, and wellness, and perform other duties as assigned.

Who We Are Looking For

You have:

Education and experience

A university degree in Mechanical, Mechatronics, Industrial, or Electrical Engineering, or an equivalent combination of education and experience.
10+ years of progressive experience in the production of complex electromechanical products, including 4+ years in an ISO 13485, FDA-regulated, or equivalent quality environment.
4+ years leading manufacturing programs from early customer engagement through design transfer, production, and sustainment.
Experience leading a team, with the results and the references to show for it.

Manufacturing readiness and quality

Hands-on experience with design transfer, process validation (IQ, OQ, PQ), production part approval, pFMEAs, and control plans.
Working knowledge of ISO 13485, 21 CFR 820 / QMSR, and ISO 14971 as they apply to manufacturing.
Broad knowledge of manufacturing methods for mechanical, electronic, and assembled products, and the judgment to choose the right one for the volume and the risk.
Experience with change control, nonconformance, and CAPA processes, and with preparing for customer and regulatory audits.

Programs, clients, and suppliers

A record of managing scope, budget, schedule, and risk on complex programs, with the financial acumen to forecast, monitor, and report.
Proven ability to work directly with external clients and suppliers, including supplier qualification and performance management.
Competence with mechanical and electronic CAD tools, PDM or PLM systems, and project management tools such as Jira.
The discipline to keep documentation complete and current, because in regulated manufacturing the record is part of the product.

Communication and judgment

Clear written, visual, and verbal communication that engages and educates stakeholders at every level, from technicians to client executives.
Strong analytical and problem-solving skills, and the habit of gathering facts before deciding.

Strong assets, not requirements:

Direct experience manufacturing medical devices or diagnostics, including cleanroom or controlled-environment assembly.
Experience in cleantech or industrial hardware.
Supplier networks in Canada and in Asia, and experience working with offshore manufacturing partners.
Experience scoping manufacturing work and quality plans at the proposal stage.

You are someone who:

Is as comfortable in front of a client as you are on the production floor.
Takes ownership of outcomes and raises risks early, before they become problems.
Listens carefully, then acts with confidence and humility.
Communicates ideas clearly, in writing, in drawings, and in person.
Takes responsibility first and credit last.
Builds constructive relationships with people across disciplines, cultures, and time zones.
Addresses concerns and conflict directly and respectfully, with the team and with clients.
Works through uncertainty by generating options and keeping things moving.
Loves learning and helps the people around you grow.
Wants to build a high-performing team and a product that matters.

Interested in Joining Our Team?

Our people are our biggest advantage. We have a talented, motivated team and we are looking for people who want to work and grow with us. We have built our culture on openness, service, and integrity, and Inertia has been certified as a Great Place to Work® for nine consecutive years based on our practices and independent employee survey results.

If this sounds like you, learn more about our values at www.inertiapd.com. If your values fit with ours, we are off to a good start.

What We Offer

Competitive compensation and benefits are the baseline. What is harder to find is the work itself: products that reach production and the people who use them, in medical devices, diagnostics, cleantech, and industrial hardware, where getting it right matters.

You will work across the whole product journey, from first client contact through engineering, validation, and production, rather than one slice of it. You will be treated as part of the team from day one, and you will have a real say in how we build the company.

We believe in continuous growth. Our people tell us they learn more here than anywhere they have worked, and we intend to keep it that way.

You will work with a diverse group of smart, open, collaborative people who take the work seriously and themselves a little less so.

Inertia is committed to building a diverse team and a safe, inclusive workplace. We are still learning and improving, and we welcome people who want to help.

Employment Type: Full Time

Primary Work Location: Hybrid, based out of our office at 34 Kern Road, Unit 3, Toronto, Ontario, Canada. This role requires regular time on site to support builds, suppliers, and the team. Must be legally permitted to work in Canada. Occasional travel, including international travel to our Guangzhou facility and to suppliers, is required.

Compensation: We are considering candidates with a range of experience. Compensation will reflect knowledge, skills, experience, and market conditions, and is supported by external benchmarking and internal equity.

Interview Process:

Phone screening with Human Resources
Remote or in-person interview with the VP Manufacturing and an Inertia team member
In-person interview with two to three Inertia team members, where you present a past manufacturing program from engineering release through production
Offer, subject to reference checks

How to Apply: If this feels like a role and a place where you will do your best work, apply online at https://www.inertiapd.com/culture-careers/ or directly through your Inertia contact.

Learn More: Visit us at www.inertiapd.com and on LinkedIn at Inertia Group.

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More about this job

Responsibilities

Lead manufacturing programs from engineering release through design transfer, pilot build, process validation, and production. Manage scope, budget, quality, and risk while developing a team of engineers and technicians.

Requirements

Requires a university degree in engineering and 10+ years of experience in complex electromechanical product production. Must have 4+ years of experience in an ISO 13485 or FDA-regulated environment and proven leadership capabilities.

Skills

Manufacturing process knowledge
Project leadership
People leadership
ISO 13485
ISO 9001
Design transfer
Process validation
Quality management
DFM
DFA
Supplier management
Change control
CAPA
Mechanical engineering
Electromechanical products
Regulatory compliance

Benefits

Competitive compensation
Professional growth opportunities
Collaborative work environment

Visa sponsorship

Not detected in the job text

Keywords

Manufacturing
Medical devices
Diagnostics
Cleantech
Industrial hardware
ISO 13485
ISO 9001
Design transfer
Process validation
IQ
OQ
PQ
pFMEA
DMR
DHR
DFM
DFA
CAPA
Change control
Mechanical engineering
Mechatronics
Industrial engineering
Electrical engineering
CAD
PDM
PLM
Jira
Regulatory compliance
Supply chain management
Quality management system

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