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Added 11 mins ago
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Actalent

Mechanical Design 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: Nov 8, 2026
Experience: 5+ years of relevant mechanical design engineering experience.
Posting language: English · French
Posted: Oct 9, 2026

Original job description

English section of this bilingual listing.

Job Title: Mechanical Design Engineer

Job Description

The Mechanical Design Engineer leads the mechanical design and development of specialty equipment that supports API and final drug product manufacturing. This role owns projects across the complete product lifecycle, from early concept and feasibility through production release and ongoing product support, with a strong focus on regulated healthcare and life sciences environments.

Responsibilities

Lead the mechanical design and development of specialty equipment used in API and final drug product manufacturing.
Own assigned projects through the full product lifecycle, from concept generation and feasibility studies to production release and ongoing product support.
Create detailed 3D models, assemblies, engineering drawings, and technical documentation using CAD software, preferably SolidWorks.
Perform engineering analyses, including tolerance stack-ups, material selection, and design reviews to ensure robust, reliable, and manufacturable designs.
Develop and refine prototypes, and support testing, verification, validation, and qualification activities to confirm design performance and compliance.
Collaborate closely with manufacturing teams to optimize designs for production, assembly, reliability, maintainability, and serviceability.
Ensure designs comply with applicable regulatory and quality standards associated with regulated industries, including medical device, pharmaceutical, GMP, and related requirements.
Participate in risk assessments such as FMEA and design hazard analyses to identify, evaluate, and mitigate potential design risks.
Apply design controls, validation processes, and documentation practices appropriate for regulated healthcare and pharmaceutical environments.
Work cross-functionally with Quality, Manufacturing, Operations, and Regulatory teams to align design solutions with operational and compliance needs.
Contribute to continuous improvement of design processes, tools, and standards in support of advanced nuclear medicine and radiopharmaceutical manufacturing.

Essential Skills

Proven mechanical design experience delivering products through the full development lifecycle, from concept and design through testing, validation, and production.
Strong 3D CAD design experience, preferably with SolidWorks, including creation of detailed models, assemblies, and engineering drawings.
Experience designing specialty equipment, medical devices, or complex mechanical systems.
Experience working in a regulated industry such as pharmaceutical, medical device, biotech, or a similar environment.
Knowledge of GMP requirements and regulatory frameworks including FDA, Health Canada, and EMA.
Understanding of design controls and validation processes in regulated environments.
Familiarity with risk assessment methodologies such as FMEA and hazard analysis.
Ability to perform engineering analyses, including tolerance stack-ups and material selection.
Experience collaborating with cross-functional teams including Quality, Manufacturing, Operations, and Regulatory.
5+ years of relevant mechanical design engineering experience.
Bachelors degree in Mechanical Engineering or a closely related discipline.

Additional Skills & Qualifications

Experience supporting verification, validation, and qualification activities for equipment and systems.
Ability to document designs, analyses, and test results clearly and accurately for use in regulated industry submissions and audits.
Interest in collaborating within a highly specialized industry and learning from experienced subject matter experts.

This posting is for an existing vacancy.

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.

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

Lead the mechanical design and development of specialty equipment used in API and final drug product manufacturing.
Own assigned projects through the full product lifecycle, from concept generation and feasibility studies to production release and ongoing product support.
Create detailed 3D models, assemblies, engineering drawings, and technical documentation using CAD software, preferably SolidWorks.
Perform engineering analyses, including tolerance stack-ups, material selection, and design reviews to ensure robust, reliable, and manufacturable designs.
Develop and refine prototypes, and support testing, verification, validation, and qualification activities to confirm design performance and compliance.
Collaborate closely with manufacturing teams to optimize designs for production, assembly, reliability, maintainability, and serviceability.
Ensure designs comply with applicable regulatory and quality standards associated with regulated industries, including medical device, pharmaceutical, GMP, and related requirements.
Participate in risk assessments such as FMEA and design hazard analyses to identify, evaluate, and mitigate potential design risks.
Apply design controls, validation processes, and documentation practices appropriate for regulated healthcare and pharmaceutical environments.
Work cross-functionally with Quality, Manufacturing, Operations, and Regulatory teams to align design solutions with operational and compliance needs.
Contribute to continuous improvement of design processes, tools, and standards in support of advanced nuclear medicine and radiopharmaceutical manufacturing.

Essential Skills

Proven mechanical design experience delivering products through the full development lifecycle, from concept and design through testing, validation, and production.
Strong 3D CAD design experience, preferably with SolidWorks, including creation of detailed models, assemblies, and engineering drawings.
Experience designing specialty equipment, medical devices, or complex mechanical systems.
Experience working in a regulated industry such as pharmaceutical, medical device, biotech, or a similar environment.
Knowledge of GMP requirements and regulatory frameworks including FDA, Health Canada, and EMA.
Understanding of design controls and validation processes in regulated environments.
Familiarity with risk assessment methodologies such as FMEA and hazard analysis.
Ability to perform engineering analyses, including tolerance stack-ups and material selection.
Experience collaborating with cross-functional teams including Quality, Manufacturing, Operations, and Regulatory.
5+ years of relevant mechanical design engineering experience.
Bachelors degree in Mechanical Engineering or a closely related discipline.

Additional Skills & Qualifications

Experience supporting verification, validation, and qualification activities for equipment and systems.
Ability to document designs, analyses, and test results clearly and accurately for use in regulated industry submissions and audits.
Interest in collaborating within a highly specialized industry and learning from experienced subject matter experts.

This posting is for an existing vacancy.

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.

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

Lead mechanical design and development of specialty manufacturing equipment, managing projects from concept and feasibility through production release and ongoing support. Create and validate designs, assess risks, ensure regulatory compliance, and collaborate with Quality, Manufacturing, Operations, and Regulatory teams to improve manufacturability and reliability.

Requirements

Requires a bachelor’s degree in Mechanical Engineering or a closely related discipline and at least five years of relevant mechanical design experience. Candidates should have strong 3D CAD skills, preferably SolidWorks, experience with complex equipment and regulated industries, and knowledge of GMP, design controls, validation, risk assessment, and engineering analyses.

Skills

Mechanical Design
SolidWorks
3D CAD Modeling
Engineering Drawings
Product Lifecycle Management
Tolerance Stack-Ups
Material Selection
Prototyping
Verification And Validation
Equipment Qualification
GMP Compliance
Design Controls
FMEA
Risk Assessment
Cross-Functional Collaboration
Manufacturing Design Optimization

Visa sponsorship

Not detected in the job text

Keywords

Mechanical Engineering
Specialty Equipment
API Manufacturing
Drug Product Manufacturing
Radiopharmaceutical Manufacturing
Nuclear Medicine
SolidWorks
3D CAD
Engineering Drawings
Product Lifecycle
Feasibility Studies
Tolerance Stack-Ups
Material Selection
Prototyping
Testing
Verification
Validation
Equipment Qualification
GMP
FDA
Health Canada
EMA
Design Controls
FMEA
Hazard Analysis
Risk Assessment
Medical Devices
Pharmaceutical Manufacturing
Design For Manufacturability
Quality

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