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Added 10 mins ago
HT
Advanced Applications Blow Molding Specialist
Husky Technologies
Bolton, ON
- Full-time
…passion of our people around the world and their desire to lead change. At the same time, we are not afraid to expect a lot and strive for leadership in all of our key markets. We are a…
Added 10 mins ago
HT
Software Validation Technologist
Husky Technologies
Bolton, ON
- Full-time
…passion of our people around the world and their desire to lead change. At the same time, we are not afraid to expect a lot and strive for leadership in all of our key markets. We are a…
Added 10 mins ago
J
Department Manager, Water Facilities (Canada)
Jacobs
Toronto, ON
- $136,600 to $225,925 USD / year
- Full-time
Lead career development activities including skill-building, growth opportunities, succession planning, and performance management through the e3 process.
Added 10 mins ago
J
Department Manager, Water Facilities (Canada)
Jacobs
Calgary, AB
- $136,600 to $225,925 USD / year
- Full-time
Lead career development activities including skill-building, growth opportunities, succession planning, and performance management through the e3 process.
Added 10 mins ago
J
Department Manager, Water Facilities (Canada)
Jacobs
Ottawa, ON
- $136,600 to $225,925 USD / year
- Full-time
Lead career development activities including skill-building, growth opportunities, succession planning, and performance management through the e3 process.
Added 10 mins ago
J
Department Manager, Water Facilities (Canada)
Jacobs
Burnaby, BC
- $136,600 to $225,925 USD / year
- Full-time
Lead career development activities including skill-building, growth opportunities, succession planning, and performance management through the e3 process.
Added 10 mins ago
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Toronto, ON
- Full-time
Lead AI Transformation: Translate real operational bottlenecks into functional AI initiatives, including our smart-quote agent and design co-pilot, driving efficiency across quoting and…
Added 10 mins ago
E
Thanks for visiting our Job Board. Please review our open positions and apply to the positions that match your qualifications.
Evertz
Burlington, ON
- Full-time
Evertz is hiring a Project Manager to lead software upgrade (regression) projects for large-scale broadcast and media systems, including SDVN / MAGNUM environments. You will drive each…
Added 11 mins ago
GO
Category Analyst (***Reposted***)
Government of Manitoba
Winnipeg, MB
- Full-time
If you applied to the original competition that closed in August, there is no need to submit another application.
Added 11 mins ago
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Associate Director, Project Execution
EPCOR
AB · Edmonton, Alberta
- Full-time
…Distribution capital and customer programs. In this role, you will lead multidisciplinary teams and contractors to safely execute projects that support system reliability, customer growth,…
Added 26 mins ago
SL
Lead Technician
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ON · Rexdale, Ontario
- Full-time
Oversee the local use of NELLC's EAM (Enterprise Asset Management) ERP application, and maintenance facility staff to record and to track local maintenance work orders and local parts…
Added 26 mins ago
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Project Geologist
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- Full-time
…Improving Daily provides the foundation for our strategy to Lead in Gold and Grow in Copper and our purpose to Unearth Value Sustainably to Advance…
Added 26 mins ago
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Finance Specialist
UPS Supply Chain Solutions
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- Full-time
…help you become better every day. We know what it takes to lead UPS into tomorrow - people with a unique combination of skill + passion. If you have the qualities and drive to lead yourself…
Added 41 mins ago
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ON · Ontario, Canada
- $130,000 to $180,000 USD / year
- Full-time
We are looking for an experienced Salesforce Technical Architect to lead the architecture design and technical delivery of enterprise scale Salesforce solutions The role will serve as the…
Added 41 mins ago
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- Full-time
…on emerging fraud trends, analytics best practices, and the application of data-driven insights to protect the bank and its…
Added 41 mins ago
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Toronto, ON
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Added 41 mins ago
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Added 41 mins ago
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Personal Support Worker - Toronto West
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Toronto, ON
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Our online application should take about 5 to 10 minutes to complete.
Added 41 mins ago
D
Manufacturing Supervisor
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…boat building industry, and we recently expanded our scope to lead the boating industry into an electrified future. Dometic has won numerous NMMA Innovation Awards over the years and we are…
Added 41 mins ago
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In this role, you will lead the development and execution of end-to-end data validation frameworks, quality gates, defect management, and release governance. Working closely with business…
Added 41 mins ago
VH
Personal Support Worker - Toronto East
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Toronto, ON · Greater Toronto Area, Canada
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Our online application should take about 5 to 10 minutes to complete.
Added 41 mins ago
C3
Systems Engineer, Sr
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Toronto, ON
- $42 to $61.54 CAD / hour
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Project Delivery & Strategic Initiatives: Lead infrastructure design, deployment, upgrades, and migrations from planning through delivery. Evaluate technology vendors, products, and service…
Added 41 mins ago
PV
Pearle Vision - Store Manager 1 - #S473 Toronto, ON
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Toronto, ON
- Full-time
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Added 41 mins ago
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Pearl Vision - Licensed Store Manager 2 - #S474 Toronto, ON
Pearle Vision
Toronto, ON · East York, ON
- Full-time
Leads OD business partnership and co-planning.

Actalent

Manufacturing Process Engineer

Ottawa, ON, Canada

$50 to $65 CAD / hour · Contract

Apply About employer

Applications open in a new tab.

Job details

Pay: $50 to $65 CAD / hour
Job type: Contract
Apply by: Dec 2, 2026
Experience: At least 5 years of mechanical manufacturing or process engineering experience in a production environment.
Posting language: English · French
Posted: Nov 2, 2026

Original job description

English section of this bilingual listing.

Job Title: Manufacturing Process Engineer

Job Description

The Manufacturing Process Engineer supports the development, implementation, and optimization of manufacturing processes in a highly regulated environment. This role works closely with Manufacturing, Quality, Regulatory, and Operations teams to ensure that processes are safe, compliant, efficient, and production-ready, contributing directly to the advancement of nuclear medicine and the improvement of patient outcomes.

Responsibilities

Develop, implement, and continuously improve manufacturing processes and production workflows to enhance safety, quality, and efficiency.
Collaborate closely with Manufacturing, Quality, Regulatory, and Operations teams to define process and equipment requirements that meet technical and regulatory standards.
Lead process development initiatives, including process validation and continuous improvement projects, to support reliable and scalable production.
Create, update, and maintain engineering documentation such as drawings, bills of materials (BOMs), process specifications, and detailed work instructions.
Perform Process Failure Mode and Effects Analysis (PFMEA) and support risk assessments to identify, evaluate, and mitigate manufacturing risks.
Troubleshoot manufacturing issues related to tooling, fixtures, equipment, and mechanical processes, implementing corrective and preventive actions.
Support equipment installation, commissioning, qualification, and optimization to ensure robust and compliant operation.
Ensure compliance with quality systems, regulatory requirements, Good Manufacturing Practice (GMP) standards, and engineering safety principles.
Participate in root cause investigations and lead or support corrective actions and process improvement efforts to prevent recurrence of issues.
Partner with quality and regulatory teams to maintain documentation and processes that meet audit, inspection, and regulatory expectations.
Contribute engineering expertise to cross-functional project teams focused on advancing nuclear medicine technologies and healthcare solutions.

Essential Skills

At least 5 years of mechanical manufacturing or process engineering experience in a production environment.
Proven experience working in a highly regulated environment, with a strong preference for medical or pharmaceutical manufacturing.
Hands-on experience with process validation, including planning, execution, documentation, and analysis of validation activities.
Demonstrated ability to troubleshoot manufacturing processes, equipment, tooling, and fixtures, and implement effective solutions.
Experience leading or participating in continuous improvement initiatives using methodologies such as Lean and Six Sigma.
Practical experience conducting PFMEA and formal risk assessments for manufacturing processes and equipment.
Strong understanding of quality systems, GMP requirements, and regulatory compliance in a manufacturing setting.
Knowledge of engineering safety principles and their application in process and equipment design and operation.
Experience creating and maintaining manufacturing documentation, including work instructions, drawings, process specifications, and BOMs.
Ability to collaborate effectively with cross-functional teams including Manufacturing, Quality, Regulatory, and Operations.

Additional Skills & Qualifications

Experience in pharmaceutical or medical device manufacturing environments.
Familiarity with nuclear medicine or other specialized healthcare manufacturing fields.
Exposure to Lean Six Sigma tools and methodologies to drive process efficiency and waste reduction.
Strong documentation skills with attention to detail and accuracy in technical records.
Ability to contribute to long-term, multi-year projects and adapt to evolving technical and regulatory requirements.
Interest in advancing healthcare and contributing to meaningful innovation in a growing and highly specialized industry.

Job Type & Location

This is a Contract position based out of Ottawa, ON.

Pay And Benefits

The pay range for this position is $50.00 - $65.00/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

Job Type & Location

This is a Contract position based out of Ottawa, ON.

Workplace Type

This is a fully onsite position in Ottawa,ON.

À propos d'Actalent

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Use of Artificial Intelligence (AI):We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Read the full bilingual original

Develop, implement, and continuously improve manufacturing processes and production workflows to enhance safety, quality, and efficiency.
Collaborate closely with Manufacturing, Quality, Regulatory, and Operations teams to define process and equipment requirements that meet technical and regulatory standards.
Lead process development initiatives, including process validation and continuous improvement projects, to support reliable and scalable production.
Create, update, and maintain engineering documentation such as drawings, bills of materials (BOMs), process specifications, and detailed work instructions.
Perform Process Failure Mode and Effects Analysis (PFMEA) and support risk assessments to identify, evaluate, and mitigate manufacturing risks.
Troubleshoot manufacturing issues related to tooling, fixtures, equipment, and mechanical processes, implementing corrective and preventive actions.
Support equipment installation, commissioning, qualification, and optimization to ensure robust and compliant operation.
Ensure compliance with quality systems, regulatory requirements, Good Manufacturing Practice (GMP) standards, and engineering safety principles.
Participate in root cause investigations and lead or support corrective actions and process improvement efforts to prevent recurrence of issues.
Partner with quality and regulatory teams to maintain documentation and processes that meet audit, inspection, and regulatory expectations.
Contribute engineering expertise to cross-functional project teams focused on advancing nuclear medicine technologies and healthcare solutions.

Essential Skills

At least 5 years of mechanical manufacturing or process engineering experience in a production environment.
Proven experience working in a highly regulated environment, with a strong preference for medical or pharmaceutical manufacturing.
Hands-on experience with process validation, including planning, execution, documentation, and analysis of validation activities.
Demonstrated ability to troubleshoot manufacturing processes, equipment, tooling, and fixtures, and implement effective solutions.
Experience leading or participating in continuous improvement initiatives using methodologies such as Lean and Six Sigma.
Practical experience conducting PFMEA and formal risk assessments for manufacturing processes and equipment.
Strong understanding of quality systems, GMP requirements, and regulatory compliance in a manufacturing setting.
Knowledge of engineering safety principles and their application in process and equipment design and operation.
Experience creating and maintaining manufacturing documentation, including work instructions, drawings, process specifications, and BOMs.
Ability to collaborate effectively with cross-functional teams including Manufacturing, Quality, Regulatory, and Operations.

Additional Skills & Qualifications

Experience in pharmaceutical or medical device manufacturing environments.
Familiarity with nuclear medicine or other specialized healthcare manufacturing fields.
Exposure to Lean Six Sigma tools and methodologies to drive process efficiency and waste reduction.
Strong documentation skills with attention to detail and accuracy in technical records.
Ability to contribute to long-term, multi-year projects and adapt to evolving technical and regulatory requirements.
Interest in advancing healthcare and contributing to meaningful innovation in a growing and highly specialized industry.

Job Type & Location

This is a Contract position based out of Ottawa, ON.

Pay And Benefits

The pay range for this position is $50.00 - $65.00/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

Job Type & Location

This is a Contract position based out of Ottawa, ON.

Workplace Type

This is a fully onsite position in Ottawa,ON.

À propos d'Actalent

Actalent est un leader mondial dans les services dingénierie et de sciences ainsi que dans les solutions de talents. Nous aidons des entreprises visionnaires à faire progresser leurs initiatives dingénierie et de science grâce à laccès à des experts spécialisés qui favorisent léchelle, linnovation et la rapidité de mise sur le marché. Avec un réseau de près de 20 000 consultants et 5 000 clients à travers les États-Unis, le Canada, lAsie et lEurope, Actalent dessert de nombreuses entreprises du Fortune 500. Nous sommes fiers dêtre lune des 500 meilleures firmes de conception de lEngineering News-Record (ENR) pour nos services de conception en ingénierie et un lauréat du prix ClearlyRated Best of Staffing® tant pour le service client que pour les talents.

Actalent est un employeur souscrivant au principe de légalité des chances et accepte toutes les candidatures sans tenir compte de la race, du sexe, de lâge, de la couleur, de la religion, des origines nationales, du statut dancien combattant, dun handicap, de lorientation sexuelle, de lidentité sexuelle, des renseignements génétiques ou de toute autre caractéristique protégée par la loi.

Si vous souhaitez faire une demande daccommodement raisonnable, tel que la modification ou lajustement du processus de demande demploi ou dentrevue à cause dun handicap, veuillez envoyer un courriel à actalentaccommodation@actalentservices.com pour connaître dautres options daccommodement.

Ordonnance sur légalité des chances de San Francisco: Conformément à lOrdonnance sur légalité des chances de San Francisco, pour tous les postes situés dans la ville et le comté de San Francisco, nous examinerons les candidatures des personnes qualifiées ayant un casier judiciaire ou des antécédents criminels.

Utilisation de lintelligence artificielle (IA): Nous pouvons utiliser lintelligence artificielle (IA) pour soutenir certaines étapes de notre processus dembauche, notamment la recherche, la présélection et lévaluation des candidatures. LIA aide à analyser les candidatures et les qualifications, mais les décisions finales sont prises par notre équipe de recrutement. En soumettant votre candidature, vous reconnaissez et acceptez que celle-ci puisse être examinée à laide doutils dIA.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Use of Artificial Intelligence (AI):We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Apply About employer

More about this job

Responsibilities

Develop, implement, validate, and improve manufacturing processes and workflows to ensure safe, efficient, compliant, and scalable production. Create and maintain engineering documentation, assess and mitigate process risks, troubleshoot equipment and manufacturing issues, and collaborate with Manufacturing, Quality, Regulatory, and Operations teams.

Requirements

Requires at least five years of mechanical manufacturing or process engineering experience, preferably in a regulated medical or pharmaceutical environment, with hands-on process validation and manufacturing troubleshooting experience. Candidates should have experience with Lean or Six Sigma improvement initiatives, PFMEA and risk assessments, GMP and regulatory compliance, engineering documentation, and cross-functional teamwork.

Skills

Manufacturing Process Engineering
Process Development
Process Validation
Continuous Improvement
Lean
Six Sigma
PFMEA
Risk Assessment
GMP Compliance
Regulatory Compliance
Root Cause Analysis
Corrective And Preventive Actions
Equipment Commissioning And Qualification
Manufacturing Documentation
Troubleshooting
Cross-Functional Collaboration

Visa sponsorship

Not detected in the job text

Keywords

Manufacturing Process Engineering
Mechanical Manufacturing
Process Development
Process Validation
Lean
Six Sigma
PFMEA
Risk Assessment
GMP
Regulatory Compliance
Quality Systems
Root Cause Analysis
Corrective And Preventive Actions
Continuous Improvement
Equipment Installation
Commissioning
Equipment Qualification
Tooling
Fixtures
Process Specifications
Work Instructions
Engineering Drawings
Bills Of Materials
Medical Manufacturing
Pharmaceutical Manufacturing
Nuclear Medicine
Production Workflows

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