Jobs in Canada

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Added 5 hours ago
YE
Test Analyst
YAC Enterprise
Canada
- Full-time
Career progression into Senior Test Analyst, QA Engineer, Automation Engineer, QA Lead, or QA Manager roles.
Added 9 hours ago
TL
Product Engineer
The Logistics Alliance Inc.
Mississauga, ON
- Full-time
…every line yourself. You'll write the requirements, review and test what gets built, deploy it, and make sure people use…
Added 11 hours ago
PS
Senior Quality Assurance Engineer
Publicis Sapient
Toronto, ON
- $95,000 to $132,000 CAD / year
- Full-time
Open to hybrid work arrangement of 3-4 days per week from the Client offices in the downtown Toronto
Added 12 hours ago
LA
Product Engineer
Logistics Alliance
ON · Mississauga, Ontario
- Full-time
…every line yourself. You'll write the requirements, review and test what gets built, deploy it, and make sure people use…
Added 18 hours ago
YE
Test Analyst
YAC Enterprise
Canada
- Full-time
Career progression into Senior Test Analyst, QA Engineer, Automation Engineer, QA Lead, or QA Manager roles.
Added 19 hours ago
LT
Senior QA Engineer
Lorven Technologies Inc.
Toronto, ON
- Contract
Our client is looking Senior QA Engineer for Long Term project in Toronto, ON / Ottawa, ON (Hybrid) Below is the detail requirement.
Added 23 hours ago
II
Quality Engineer
Intero Integrity
Toronto, ON
- Full-time
Are you a Quality Engineer who would rather fix the root cause on the shop floor than write another procedure nobody reads? Then this new role is for you. You'll help shape how quality and…
Added 1 day ago
DI
Data Engineer – Enterprise Data Engineering, Data Science and Informatica
Data Intuition Inc.
Brampton, ON
- $47 CAD / hour
- Full-time
- Lead and coordinate information systems professionals and data administrators.
Added 1 day ago
T
Sr. Angular Engineer
Telna
ON · Ontario, Canada
- Full-time
Set the standard for unit and integration testing, and keep a healthy test pyramid with fast unit tests, component tests and a focused set of end-to-end tests.
Added 1 day ago
H
Senior QA Engineer
Hays
Vancouver, BC
- Contract
The client’s digital team is looking for a Senior QA Engineer with experience across our in-store Point-of-Sale (POS) and mobility stack, including Oracle Xstore and Xmobile, to support…
Added 1 day ago
VL
Lead QA Engineer
VStream Labs Inc.
Toronto, ON
- Contract
VStream Labs Inc. is seeking a Lead QA Engineer with 5+ years of experience in software quality assurance, test automation, and end-to-end testing. You will lead QA activities, define…
Added 1 day ago
D
Senior SDET / Quality Engineering Lead/Architect
Droisys
Brampton, ON
- Contract
We are seeking a Senior Software Development Engineer in Test (SDET) / Quality Engineering Architect to join our team. The ideal candidate will have strong experience in architecting…
Added 1 day ago
CL
Quality Assurance Automation Engineer
Cloudious LLC
Toronto, ON
- Contract
Lead end-to-end testing activities, including test planning, execution, defect management, and delivery ownership.
Added 2 days ago
MC
Technical Consultant III (35732)
Myticas Consulting
Toronto, ON
- Full-time
Technical Consultant III (Software Engineer, Senior/Lead)
Added 2 days ago
MC
Senior QA Engineer III – Automation | Banking | API | Kafka | ETL (35729)
Myticas Consulting
Ottawa, ON
- Full-time
We are seeking a Senior QA Engineer III with strong hands-on test automation and banking/financial services experience to support complex enterprise applications and integration…
Added 2 days ago
D
Software Engineer in Test
Dexian
Mississauga, ON
- Other
We are seeking a visionary and hands-on Senior Software Development Engineer in Test (SDET)/Quality Engineering Architect to define, champion, and drive the global quality engineering…
Added 2 days ago
BI
Quality Engineer I, QA Systems
Baxter International Inc.
Alliston, ON
- Full-time
As a Quality Engineer, you will serve as a key technical expert responsible for ensuring manufacturing systems, equipment, and processes meet regulatory, quality, and data integrity…
Added 2 days ago
BC
Test Analyst
BK CONSULTING GABON
Canada
- Full-time
Career progression into Senior Test Analyst, QA Engineer, Automation Engineer, QA Lead, or QA Manager roles.
Added 2 days ago
HS
Quality Supervisor
HR Solutions
ON · Niagara, ON
- Full-time
 Certified Quality Engineer/Certified Quality Technician preferred, Certified Manager of
Added 2 days ago
MA
Solutions Engineer
Mosaic AI
Toronto, ON
- Full-time
We’re hiring a Solutions Engineer to own the technical and operational success of our customers from pre-sale through post-sale. This is a full-lifecycle role: you’ll run POVs, lead…
Added 4 days ago
SC
Test Analyst
Sustainability consulting
Canada
- Full-time
Career progression into Senior Test Analyst, QA Engineer, Automation Engineer, QA Lead, or QA Manager roles.
Added 4 days ago
Supplier Quality Engineer
Westerkirk
Calgary, AB
The Supplier Quality Engineer reports to the Director of Quality for Manufacturing and the primary purpose of the role is to; develop, implement, and coordinate the supplier approval…
Added 5 days ago
TI
AI Software Development Engineer in Test
Trimble Inc.
Kamloops, BC
- Full-time
Location: Kamloos, Canada (Onsite - Four Days Per Week)
Added 5 days ago
BE
MPD Technology - Automation Manager
Beyond Energy Services and Technology Corp.
Calgary, AB
- Full-time
Manage vendor relationships, technical bid evaluation, lead times, obsolescence and spares strategy.
Added 5 days ago
MPD Technology - Automation Manager
Beyond Energy Services & Technology
Calgary, AB
Manage vendor relationships, technical bid evaluation, lead times, obsolescence and spares strategy.

Baxter International Inc.

Quality Engineer I, QA Systems

Alliston, ON, Canada

Full-time

Apply on baxter.wd1.myworkdayjobs.com About employer

Applications open in a new tab.

Job details

Job type: Full-time
Apply by: Nov 16, 2026
Experience: 5+ years of validation experience within a GMP-regulated pharmaceutical, biotechnology, medical device, or healthcare manufacturing environment.
Posting language: English
Posted: Nov 9, 2026

Original job description

This is where your work makes a difference.

At Baxter, we believe every person - regardless of who they are or where they are from - deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond.

Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results.

Here, you will find more than just a job - you will find purpose and pride.

Your Role at Baxter

As a Quality Engineer, you will serve as a key technical expert responsible for ensuring manufacturing systems, equipment, and processes meet regulatory, quality, and data integrity requirements. You will lead validation initiatives that enable reliable product quality, support continuous improvement, and help maintain inspection readiness in a highly regulated healthcare manufacturing environment.

In this role, you will collaborate across multiple functions to develop and execute validation strategies, provide technical guidance, support change management activities, and help ensure the site remains compliant with Health Canada, GMP, ISO, and corporate quality standards. Your expertise will help safeguard patient safety while enabling innovation and operational excellence.

What You'll Be Doing

Lead the development, execution, and completion of validation programs for manufacturing equipment, processes, cleaning and computerized systems to ensure a validated state of control.
Author validation protocols and reports, analyze validation data, and apply statistical techniques to demonstrate compliance with regulatory and quality requirements.
Partner with Engineering, Production, Quality Control, and external vendors to plan, coordinate, and execute qualification activities including IQ, OQ, and PQ protocols.
Serve as a validation subject matter expert by providing technical guidance on process validation, cleaning validation, equipment qualification, computerized systems validation, and data integrity practices.
Support change control and quality system activities by assessing validation impacts, contributing to investigations, and leading resolution of validation-related non-conformances and corrective actions.
Participate in internal audits, regulatory inspections, and compliance activities while helping ensure ongoing readiness and adherence to applicable standards.
Drive continuous improvement initiatives by identifying opportunities to strengthen validation processes, improve efficiency, and support Baxter's operational excellence objectives.

What You'll Bring

Required Qualifications

Bachelor's degree in engineering, Chemistry, Microbiology, Pharmacy, Life Sciences, or a related scientific discipline.
5+ years of validation experience within a GMP-regulated pharmaceutical, biotechnology, medical device, or healthcare manufacturing environment.
Experience executing equipment qualification, process validation, cleaning validation and computerized systems validation, or test method validation activities.
Working knowledge of GMP regulations, PICs, ISO standards, data integrity requirements, and regulatory compliance expectations.
Strong technical writing skills with experience developing protocols, reports, investigations, technical assessments, and validation documentation.
Demonstrated ability to manage multiple projects while collaborating effectively with cross-functional teams.
Strong analytical, problem-solving, and critical-thinking skills, including experience interpreting validation data and applying statistical tools.
Effective communication and relationship-building skills with the ability to influence stakeholders across all levels of the organization.

Preferred Qualifications

Experience supporting pharmaceutical manufacturing operations or liquid processing systems.
Knowledge of Health Canada regulations and experience supporting regulatory inspections.
Experience with TrackWise Change Management and CAPA systems.
Working knowledge of Minitab, Statistical Process Control (SPC), and data analysis methodologies.
Lean Manufacturing, Continuous Improvement, or Six Sigma Green Belt certification.
Experience supporting commissioning activities, technical investigations, and root cause analysis initiatives.
Familiarity with Baxter or similar corporate quality systems and validation requirements.
Experience working with ERP systems

We understand that compensation is an important factor as you consider the next step in your career. At Baxter, we are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. The estimated salary range for this position is $72,080.00 - $108,120.00 CAD annually, which reflects base salary as well as estimated target payout under the Management Incentive Compensation Plan. Individual pay will be determined based upon skills, expertise and experience, and the incentive, which is contingent upon company and individual performance outcomes. For questions about this, our pay philosophy, and available benefits, please speak to the recruiter if you decide to apply and are selected for an interview.

This posting is for a current existing vacancy within our organization. We are actively seeking qualified candidates to fill this open position. If you are interviewed for this position, we will advise you within 45 days of the interview as to whether or not you were successful in obtaining the position. Information submitted as part of the job application process will be kept on file for 3 years from the date of submission in accordance with legislative requirements.

As part of our recruitment process, Baxter Corporation may use AI tools to assist screening candidates and assist in evaluating candidate qualifications. All final hiring decisions are made by the hiring manager and recruitment team

Equal Employment Opportunity

Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.

Reasonable Accommodations

Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.

Recruitment Fraud Notice

Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.

Apply on baxter.wd1.myworkdayjobs.com About employer

More about this job

Responsibilities

The Quality Engineer will lead validation programs for manufacturing equipment, processes, and computerized systems to ensure regulatory compliance and operational excellence. They will collaborate with cross-functional teams to execute protocols, manage change control, and support internal audits and regulatory inspections.

Requirements

Candidates must hold a bachelor's degree in a scientific or engineering discipline and possess at least 5 years of validation experience in a GMP-regulated environment. Strong technical writing, analytical skills, and a working knowledge of regulatory standards like ISO and Health Canada are required.

Skills

Validation
GMP
Quality Engineering
Technical Writing
Data Integrity
Equipment Qualification
Process Validation
Cleaning Validation
Computerized Systems Validation
Regulatory Compliance
Statistical Analysis
Change Management
CAPA
Root Cause Analysis
ISO Standards
Project Management

Visa sponsorship

Not detected in the job text

Keywords

Validation
GMP
Quality Engineering
Health Canada
ISO Standards
Data Integrity
IQ
OQ
PQ
Technical Writing
Change Management
CAPA
Minitab
Statistical Process Control
Lean Manufacturing
Six Sigma
Root Cause Analysis
Pharmaceutical
Biotechnology
Medical Device
Manufacturing
Compliance
Regulatory Affairs
Validation Protocols
Cleaning Validation
Computerized Systems Validation
ERP Systems
Quality Control
Operational Excellence
Risk Assessment

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Jobs in Canada