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Added 3 mins ago
BI
Connected Vitals Account Manager
Baxter International Inc.
AB · Vancouver, BC · Calgary, AB
- Full-time
Lead seamless transitions from the sales process to implementation by partnering with project management and clinical implementation teams.
Added 3 mins ago
E
Senior Manager, Data Science & Analytics
eBay
Toronto, ON
- Full-time
We are seeking an inspiring Senior Manager, Data Science & Analytics to lead our dynamic team in San Jose. In this role, you will be a technical leader with vision and a domain pioneer. You…
Added 4 mins ago
SH
Personal Support Worker
SE Health
North Middlesex, ON
- Full-time
…exceptional care to people and communities across Canada. We lead with empathy, dignity and purpose while building a future where everyone can realize their full health and well-being…
Added 4 mins ago
SH
Personal Support Worker
SE Health
London, ON
- Full-time
…clinician, a member of the interdisciplinary team who will lead care planning for that client and facilitate interdisciplinary team to reach client’s care goals. As part of the SE…
Added 4 mins ago
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Senior Strategist, Enterprise
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Toronto, ON
- Full-time
This is transformation work, and at this level you will own significant parts of it. You will lead discovery, form the point of view on where a client stands and where they need to be, and…
Added 4 mins ago
IF
Senior Compliance Associate - Automation & Systems
Ink Foundation
Canada
- Full-time
Lead transaction monitoring optimization, including rule testing, threshold tuning, and the design and rollout of new monitoring scenarios to improve detection quality and reduce false…
Added 4 mins ago
Sr Architect
Insight Enterprises, Inc.
Toronto, ON
Design and lead modern data architectures that support analytics, business intelligence, machine learning, and AI-driven use cases.
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D
Assistant Manager, Yardi Implementation, Finance Operations Advisory
Deloitte
Toronto, ON
- Full-time
You will lead or coordinate key components of the implementation lifecycle, including requirements gathering, business process and fit-gap analysis, solution design, system configuration,…
Added 4 mins ago
IC
Sourcing Specialist- EN
IAMGOLD Corporation
Gogama, ON
- Full-time
We're actively searching for a Sourcing Specialist, reporting to the Senior Sourcing Lead. This role supports the commercial execution and ongoing management of agreements and partnerships,…
Added 4 mins ago
ZS
GCP Architect
Zortech Solutions
Canada
- Contract
8+ years in cloud architecture roles, with at least 3 years specifically on Google Cloud Platform in an architect or lead capacity.
Added 4 mins ago
IF
Sales Operations Analyst - Payward Services
Ink Foundation
Canada
- Full-time
Lead internal preparation and alignment for major client presentations, particularly RFP due diligence meetings, and track action items through to resolution
Added 4 mins ago
IF
Staff Brand Designer - Consumer
Ink Foundation
Canada
- Full-time
You report to the Creative Lead, Consumer Creative & Design, who gives you direction, feedback and cover in reviews. This is a senior individual contributor role with no direct reports.…
Added 4 mins ago
IF
Staff Product Designer - AI Products
Ink Foundation
Canada
- Full-time
Forget crypto. Fintech/crypto are now one of the same. Come join us to lead Product Design for the building of elite AI products, end-to-end. A personal finance agent that shapes how people…
Added 4 mins ago
IF
Senior Analytics Engineer - Finance
Ink Foundation
Canada
- Full-time
Judgment and autonomy to lead complex work, navigate ambiguity and remain accountable for production outcomes.
Added 4 mins ago
IF
Senior Video Creative, Performance - Kraken Consumer
Ink Foundation
Canada
- Full-time
You report to the Creative Lead, Consumer Creative & Design, who gives you direction, feedback and cover in reviews. This is a senior individual contributor role with no direct reports.…
Added 4 mins ago
D
Senior Analyst, Global Vendor Management
Deloitte
Toronto, ON
- Full-time
…professionals reach across disciplines and borders to develop and lead global initiatives. We deliver strategic programs and services that unite our…
Added 4 mins ago
IF
Head of Organic Growth, Kraken Pro
Ink Foundation
Canada
- Full-time
Lead a lean, scrappy team. Set direction, coach, and unblock a small team, while staying hands-on enough to ship, test, and fix things yourself.
Added 4 mins ago
AS
Quality Engineer
AgileGrid Solutions
Canada
- Full-time
Troubleshoot product failures and lead investigations to identify root causes.
Added 4 mins ago
GC
Account Manager, Security Master Supervisor
Guardian Capital Group
Toronto, ON
- Full-time
Lead, coach, and develop a team of analysts and senior analysts.
Added 4 mins ago
IF
Lead, Business Operations - Payward Services
Ink Foundation
Canada
- Full-time
As a Lead, Business Operations, you’ll be the operating generalist for PWS. Your core is partner launch and the operating rhythm behind the business, and from there you’ll take on whatever…
Added 4 mins ago
A
Agent Method // Methods Agent
Actalent
Mirabel, QC
- $35 to $60 CAD / hour
- Contract
Lead project follow-up meetings and keep tracking files up to date.
Added 4 mins ago
CL
Human Resources - HR Business Partner
Cosmetica Laboratories Inc
Toronto, ON · Scarborough, ON
- Full-time
Added 4 mins ago
LM
Senior Surety Claims Counsel OR Senior Surety Claims Expert
Liberty Mutual Canada
Toronto, ON
- Full-time
The Senior Counsel will lead the investigation, evaluation, negotiation, and resolution of sophisticated surety claims that often involve construction project completion, contract disputes,…
Added 4 mins ago
A
Sale Support Specialist
ABB
Coquitlam, BC
- Full-time
At ABB, we help industries run leaner and cleaner - and every person here makes that happen. You’ll be empowered to lead, supported to grow, and proud of the impact we create together. Join…
Added 4 mins ago
D
Software Engineer in Test
Dexian
Mississauga, ON
- Other
In this role, you will lead the technical vision for automated quality gates, design scalable test automation frameworks from scratch, integrate cutting-edge AI-driven testing tooling, and…

Baxter International Inc.

Quality Engineer I, QA Systems

Alliston, ON, Canada

Full-time

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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.

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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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