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Added 47 mins ago
Night Supervisor, Maintenance
CONA Services
Brampton, ON
…Maintenance department to ensure the eﬃciency of the highest quality product at the lowest cost, while meeting customer…
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Evaluate supplier quality system maturity and performance through audits, assessments, and quality metrics, identifying opportunities for improvement and strengthening supplier capabilities.
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Lead Full Stack Engineer
Manulife
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Senior Product Engineer
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Job Title: Quality Engineer (QE) / SDET – AI Chatbot Validation
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Propose product evolutions/process improvement axes.
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Added 5 hours ago
'
Process Engineer
''
Carberry, MB
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McCain Foods (Canada) has an immediate opening for a Process Engineer at our Carberry, Manitoba Food Processing Plant. This role reports to the Production Manager. This role makes sure the…
Added 5 hours ago
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Expert AI Engineering-CA
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Added 5 hours ago
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Quality Engineer (QE) / SDET – AI Chatbot Validation
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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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