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Added 1 min ago
PH
Quality Assurance and Compliance Coordinator
Providence Healthcare
Vancouver, BC
- Part-time
…physiotherapists, social workers, pharmacists – form a dedicated team committed to improving the lives of people living with kidney disease. Providence Health Care also operates seven…
Added 1 min ago
C
Head of Sales
Chatbase
Toronto, ON
- $290,000 to $380,000 CAD / year
- Full-time
This is a player-coach role reporting to Humphrey Su, our Head of GTM. You'll carry your own number from day one, and you'll hire and lead our AE team as it grows.
Added 1 min ago
C
Partnerships Lead, Startups & Channel
Chatbase
Toronto, ON
- Full-time
…self-serve, and now we're moving upmarket and building our sales team. Partnerships are the biggest growth lever we haven't pulled yet. You'll own all of…
Added 1 min ago
C
GTM Engineer
Chatbase
Toronto, ON
- $110,000 to $160,000 CAD / year
- Full-time
…self-serve, and now we're moving upmarket and building our sales team. We have a lot of inbound and almost no outbound machine yet. You'll build…
Added 1 min ago
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BDR Manager
Chatbase
Toronto, ON
- $145,000 to $195,000 CAD / year
- Full-time
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Added 17 mins ago
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Florist Assistant
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Oakville, ON
- Full-time
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Added 17 mins ago
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Flight Physics Integrator / Intégrateur physiques du vol
Airbus Aircraft
Montreal, QC
- Full-time
The A220 commercial aircraft Programme is looking for a New Development Flight Physics Integrator to join our engineering team based in Mirabel (Québec, Canada).
Added 47 mins ago
CC
Planner, Mobile Maintenance
Cameco Corporation
SK · Saskatchewan, Canada
- Full-time
As a member of the maintenance planning team, reporting to the senior planner, you will be committed towards helping McArther River reach reliability excellence. You will build…
Added 47 mins ago
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Planner, Stationary Maintenance
Cameco Corporation
SK · Saskatchewan, Canada
- Full-time
As a member of the maintenance planning team, reporting to the senior planner, you will be committed towards helping McArther River reach reliability excellence. You will build…
Added 47 mins ago
TC
Retail Store Coordinator Full Time Winners Duncan Mall
TJX Canada – Winners, Marshalls, HomeSense
Duncan, BC
- Full-time
We’re looking for a Retail Store Coordinator to join our team in a welcoming environment. In this role, you’ll lead and inspire to deliver outstanding customer experiences. If you thrive in…
Added 47 mins ago
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(CAN) Fashion Team Lead
Walmart Canada
Calgary, AB
- Full-time
…communicated priorities from the Coach and the Store Management Team. Delegate, assist and follow-up on completion of daily Customer Availability process…
Added 47 mins ago
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(CAN) Fashion Team Lead
Walmart
Calgary, AB
- Full-time
…communicated priorities from the Coach and the Store Management Team. Delegate, assist and follow-up on completion of daily Customer Availability process…
Added 1 hour ago
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Project Manager
PTW Energy Services
Nisku, AB
- Full-time
PTW is always looking for talented professionals to join our team. If you're interested in a career with PTW, we encourage you to apply and connect with us about current and future…
Added 1 hour ago
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Specialist Occupational Therapist
NHS Scotland
Kawartha Lakes, ON
- Full-time
…the vibrant, forward thinking Allied Health Professions (AHP) team providing Secure Care services at the Rohallion Clinic, Murray Royal Hospital, Perth. Rohallion represents a unique…
Added 1 hour ago
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Welding Shop Supervisor
Platinum Trailers
St. Marys, ON
- $32 to $40 CAD / hour
- Full-time
Leadership: 2+ years of experience in a supervisory, team lead, or lead hand role within a fabrication shop.
Added 1 hour ago
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Overnight Lead Department Manager
Walmart Canada
Thunder Bay, ON
- Full-time
Position Summary...Working as an Overnight Lead Department Manager at Walmart Canada is a great opportunity to build leadership experience in a fast‑paced retail environment. In this role,…
Added 1 hour ago
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Merchandising Coordinator
TJX Canada – Winners, Marshalls, HomeSense
Lethbridge, AB
- Full-time
We’re looking for a Retail Store Coordinator to join our team in a welcoming environment. In this role, you’ll lead and inspire to deliver outstanding customer experiences. If you thrive in…
Added 1 hour ago
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Project Engineer
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- Full-time
Lead all stages of development, including site selection, power sourcing, and financial modelling.
Added 1 hour ago
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Director of Business Development
Creative Clicks
Toronto, ON
- Full-time
Recruit, coach and lead an initial team of two to three Business Developers.
Added 1 hour ago
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HSE Site Representative
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- Full-time
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MLHD - Visiting Medical Officer - Orthopaedic Surgery (Apply via eCredential)
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Griffith, ON
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Lead excellence in orthopaedic surgery while supporting the next generation of clinicians.
Added 1 hour ago
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Project Operations Manager (Construction)
Jobgether
Canada
- $85,000 to $105,000 CAD / year
- Full-time
…accountability throughout the project lifecycle. You will also lead a project coordinator and strengthen processes, systems, and workflows to improve efficiency and consistency. The ideal…
Added 1 hour ago
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HSE Site Representative
WSP in Canada
ON · Ontario, Canada
- Full-time
…the Northwest Territories. Working as part of the WSP field team and reporting to the Project Manager, you’ll provide hands-on health and safety support to crews while helping ensure work…
Added 1 hour ago
WI
HSE Site Representative
WSP in Canada
Quebec, QC
- Full-time
…the Northwest Territories. Working as part of the WSP field team and reporting to the Project Manager, you’ll provide hands-on health and safety support to crews while helping ensure work…
Added 1 hour ago
WI
HSE Site Representative
WSP in Canada
Quebec, QC
- Full-time
…the Northwest Territories. Working as part of the WSP field team and reporting to the Project Manager, you’ll provide hands-on health and safety support to crews while helping ensure work…

Actalent

Validation Specialist

Cambridge, ON, Canada

$35 to $50 CAD / hour · Contract

Apply About employer

Applications open in a new tab.

Job details

Pay: $35 to $50 CAD / hour
Job type: Contract
Apply by: Nov 25, 2026
Experience: 3+ years of validation engineering experience in a GMP-regulated environment.
Posting language: English · French
Posted: Oct 27, 2026

Original job description

English section of this bilingual listing.

Overview

We are seeking a Validation Specialist to support the qualification and validation of automated manufacturing equipment used in GMP-regulated Life Science environments. This role is responsible for developing and executing validation activities, creating IQ/OQ/PQ documentation, and serving as the primary validation contact throughout project execution.

Key Responsibilities

Develop and execute validation plans, protocols, and reports for automated equipment and production systems.
Perform IQ, OQ, and PQ activities in accordance with GMP and Life Science Validation requirements.
Collaborate with engineering teams to create validation documentation and functional specifications.
Review electrical schematics, drawings, and wiring to verify proper installation and functionality.
Conduct equipment testing for PLCs, HMIs, VFDs, vision systems, instrumentation, motors, and pneumatic/hydraulic systems.
Verify electrical utilities, perform continuity testing, and support troubleshooting activities.
Act as the primary validation lead for assigned projects and coordinate validation activities across project teams.

Qualifications

Bachelor's degree in Engineering, Physics, Chemistry, Life Sciences, or a related field, or equivalent experience.
3+ years of validation engineering experience in a GMP-regulated environment.
Hands-on experience with IQ/OQ/PQ execution and validation documentation.
Strong understanding of GMP, CQV, and Life Science Validation principles.
Experience working with automated production equipment and PLC-based control systems.
Ability to read and interpret electrical schematics and technical drawings.
Experience with calibration, electrical testing, and industrial control systems.
Strong technical writing, communication, and organizational skills.

Preferred Qualifications

Experience within pharmaceutical, biotechnology, medical device, or other regulated manufacturing industries.
Experience leading customer-facing validation projects and documentation reviews.
Familiarity with industrial safety systems and machine qualification activities.

Work Environment

This position combines hands-on equipment qualification with documentation and project coordination. The role works closely with engineering, automation, and customer teams in office and manufacturing environments, with occasional travel to customer sites as required.

Job Type & Location

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

Pay And Benefits

The pay range for this position is $35.00 - $50.00/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 Cambridge, ON.

Workplace Type

This is a fully onsite position in Cambridge,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 and execute validation plans, protocols, and reports for automated equipment and production systems.
Perform IQ, OQ, and PQ activities in accordance with GMP and Life Science Validation requirements.
Collaborate with engineering teams to create validation documentation and functional specifications.
Review electrical schematics, drawings, and wiring to verify proper installation and functionality.
Conduct equipment testing for PLCs, HMIs, VFDs, vision systems, instrumentation, motors, and pneumatic/hydraulic systems.
Verify electrical utilities, perform continuity testing, and support troubleshooting activities.
Lead deviation investigations, change controls, and validation documentation updates.
Facilitate internal and customer validation reviews.
Act as the primary validation lead for assigned projects and coordinate validation activities across project teams.

Qualifications

Bachelor's degree in Engineering, Physics, Chemistry, Life Sciences, or a related field, or equivalent experience.
3+ years of validation engineering experience in a GMP-regulated environment.
Hands-on experience with IQ/OQ/PQ execution and validation documentation.
Strong understanding of GMP, CQV, and Life Science Validation principles.
Experience working with automated production equipment and PLC-based control systems.
Ability to read and interpret electrical schematics and technical drawings.
Experience with calibration, electrical testing, and industrial control systems.
Strong technical writing, communication, and organizational skills.

Preferred Qualifications

Experience within pharmaceutical, biotechnology, medical device, or other regulated manufacturing industries.
Experience leading customer-facing validation projects and documentation reviews.
Familiarity with industrial safety systems and machine qualification activities.

Work Environment

This position combines hands-on equipment qualification with documentation and project coordination. The role works closely with engineering, automation, and customer teams in office and manufacturing environments, with occasional travel to customer sites as required.

Job Type & Location

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

Pay And Benefits

The pay range for this position is $35.00 - $50.00/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 Cambridge, ON.

Workplace Type

This is a fully onsite position in Cambridge,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 and execute validation plans, protocols, and reports, including IQ/OQ/PQ activities, for automated manufacturing equipment and production systems in GMP-regulated environments. Lead validation activities for assigned projects, coordinate with engineering and customer teams, test equipment and electrical systems, and manage deviations, change controls, and documentation reviews.

Requirements

Requires a bachelor's degree in engineering, physics, chemistry, life sciences, or a related field, or equivalent experience, and at least three years of validation engineering experience in a GMP-regulated environment. Candidates should have hands-on IQ/OQ/PQ and validation documentation experience, knowledge of GMP and CQV, familiarity with automated equipment and PLC systems, and the ability to interpret electrical schematics and technical drawings.

Skills

Validation Planning
IQ/OQ/PQ Execution
GMP Compliance
Life Science Validation
Commissioning, Qualification, And Validation (CQV)
Validation Documentation
Automated Manufacturing Equipment
PLC-Based Control Systems
Electrical Schematics
Technical Drawings
Calibration
Electrical Testing
Deviation Investigations
Change Control
Technical Writing
Project Coordination

Visa sponsorship

Not detected in the job text

Keywords

GMP
Life Sciences
Commissioning, Qualification, And Validation (CQV)
IQ
OQ
PQ
Validation Plans
Validation Protocols
Validation Reports
Automated Manufacturing Equipment
Production Systems
PLC
HMI
VFD
Vision Systems
Instrumentation
Electrical Schematics
Technical Drawings
Calibration
Electrical Utilities
Continuity Testing
Troubleshooting
Deviation Investigations
Change Control
Industrial Control Systems
Machine Qualification
Industrial Safety Systems
Pharmaceutical Manufacturing
Biotechnology
Medical Devices

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