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Added 24 mins ago
DO
Project Coordinator, Practice Transformation
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- Full-time
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STEMCELL Technologies

Manager, Validation Engineering

Burnaby, BC, Canada
Canada - BC, Burnaby, Production Way, Onsite, Canada

$116,700.00 - $175,100.00 · Full-time

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Job details

Pay: $116,700.00 - $175,100.00
Job type: Full-time
Posting language: English
Posted: Oct 29, 2026

Original job description

Job Description Summary

Are you a driven validation leader ready to shape quality standards and drive engineering excellence across complex operations? Join STEMCELL Technologies as the Manager, Validation Engineering, where you will lead a dynamic team, oversee robust Quality Assurance Validation strategies, and ensure seamless regulatory compliance at Canada’s largest biotechnology company!

In this key leadership role, you will provide critical cross-functional guidance, align validation practices with industry standards, and mentor engineering professionals. You will collaborate closely with cross-departmental teams to champion innovative validation frameworks and uphold the highest quality and safety benchmarks across our facilities.

If you’re a strategic thinker and proactive leader who excels in high-stakes compliance and thrives in a collaborative, fast-paced environment, we want to hear from you!

Job Description

Duties and Responsibilities

Leads, directs and reviews the work of quality validation engineers, establishes annual goals and performance standards, identifies training needs, and recommends adjustments to training materials
Oversees and maintains Quality Management Systems (QMS), operational standards, and procedural controls necessary for the Commissioning, Qualification and Validation (CQV)
Directs continuous improvement within quality assurance (QA) processes by monitoring and evaluating metrics and key performance indicators (KPIs) to analyze effectiveness, recognize trends, and implement operational enhancements
Manages technical guidance and resource allocation across project teams engaged in multidisciplinary product development, lifecycle management, and design control
Collaborates cross-functionally to integrate quality knowledge and compliance protocols into business operations and effectively resolves complex quality issues

Knowledge and Qualifications

Bachelor’s degree in Sciences or Engineering with a minimum of 8 years of progressive experience in quality assurance in a regulated industry
1 to 3 years of direct experience leading, supervising, or mentoring teams
Specialized and extensive knowledge of Quality System regulatory requirements (ISO 13485, ISO 9001, and FDA 21 CFR regulations)
Demonstrated practical experience implementing, managing, and auditing QMS, with experience in Computer System Validation is an asset
Proven ability to balance regulatory compliance with business and operational requirements

#Nonbench

STEMCELL Technologies is a privately owned, Vancouver-based biotechnology company that helps power leading-edge life science research around the world. Driven by our love of science and passion for quality, we are a company of Scientists Helping Scientists - standing by our customers to provide the outstanding products, technical support, and training they need to advance their research. Scientists performing stem cell, immunology, cancer, regenerative medicine, and cellular therapy research are among those who rely on our cell culture media, cell separation products, instruments, accessory products, and services. Through our many regional offices, as well as our distribution centers in Vancouver, Seattle, Grenoble, and Singapore, we deliver our innovative, specialized products to more than 100 countries. With over 1,800 employees globally, most with scientific or engineering degrees, STEMCELL is proud to be the largest biotechnology employer in Canada.

This is an opportunity to work with highly motivated colleagues in a science-oriented, creative, and dynamic environment. We offer a competitive salary, excellent benefits, and meaningful career development opportunities.

STEMCELL is well recognized for exceptional leadership and business practices. We are one of Canada’s Best Managed Companies and operate an ISO 14001-certified environmental management system to measure and reduce our environmental impact.

As an equal opportunity employer, STEMCELL is dedicated to ensuring that every employee feels safe, valued, and respected for who they are. We know that scientific progress and innovation occur when diverse, creative minds come together and we are committed to nurturing a culture of inclusivity and belonging. STEMCELL enforces a zero-tolerance policy for any form of discrimination. Selection decisions are solely based on job-related factors.

The annual salary for this job ranges from:

$116,700.00 - $175,100.00

STEMCELL determines an individual’s pay within the range based on multiple factors including experience, education, job-related skills, and equity within the team or organization. For jobs that are eligible for sales incentives, the range noted above is inclusive of target incentives; actual incentives are based on individual performance results in accordance with company policy. In addition to base salary, STEMCELL offers a comprehensive total rewards package including health benefits, retirement savings, and more.

To apply, please select the “Apply” button below. You will then be directed to a login screen asking you to set up an account, which is required to apply.

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More about this job

Responsibilities

The Manager of Validation Engineering leads a team to oversee quality assurance strategies, regulatory compliance, and commissioning, qualification, and validation (CQV) processes. They also drive continuous improvement initiatives and provide cross-functional guidance to ensure engineering excellence across all operations.

Requirements

Candidates must hold a Bachelor's degree in Sciences or Engineering and possess at least 8 years of progressive experience in quality assurance within a regulated industry. Additionally, 1 to 3 years of direct leadership experience and extensive knowledge of ISO and FDA regulatory requirements are required.

Skills

Quality assurance
Validation engineering
Regulatory compliance
ISO 13485
ISO 9001
FDA 21 CFR
Quality management systems
Commissioning, qualification and validation
Team leadership
Mentoring
Computer system validation
Continuous improvement
Design control
Lifecycle management
Strategic planning
Risk management

Benefits

Health benefits
Retirement savings
Career development opportunities

Visa sponsorship

Not detected in the job text

Keywords

Validation Engineering
Quality Assurance
Biotechnology
ISO 13485
ISO 9001
FDA 21 CFR
CQV
QMS
Regulatory Compliance
Computer System Validation
Engineering Leadership
KPIs
Design Control
Lifecycle Management
Operational Standards
STEMCELL Technologies
Life Science Research
Quality Management Systems
Process Improvement
Technical Guidance

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