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Added 2 days ago
B
PRINCIPAL, VENTURE CAPITAL - Thrive Venture Fund
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- Full-time
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- Full-time
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Added 6 days ago
ST
Quality Engineer, Validation
STEMCELL Technologies
Burnaby, BC · Canada - BC, Burnaby, Production Way (ABMF), Onsite
- Full-time
Educate, train, advise and coach other employees to ensure adherence to all applicable quality standards for assigned areas
Added 9 days ago
M
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- Full-time
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Added 10 days ago
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Added 10 days ago
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Senior Director, Travel Operations & Customer Experience
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Toronto, ON
- Full-time
…over $4.5 billion in annual travel sales. All our investments stem from a common thesis, that travel advisors add real value to a trip. Travel advisors when equipped with technology and…
Added 12 days ago
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Treasury Associate Program
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Added 17 days ago
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Biomarker & Bioanalytical Development Lead (Director / Senior Director)
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Vancouver, BC
- Full-time
…and tissues (e.g., hybridization ELISA, LC-MS/MS, LC-HRMS, stem-loop RT-qPCR) to support PK, tissue distribution, and exposure–response…
Added 19 days ago
Manager - Risk, Process & Controls - French Bilingual
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Added 23 days ago
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Added 23 days ago
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Canada
- Full-time
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Added 24 days ago
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Added 25 days ago
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Added 1 month ago
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Manager, Engineering
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STEMCELL Technologies

Quality Engineer, Validation

Burnaby, BC, Canada
Canada - BC, Burnaby, Production Way (ABMF), Onsite, Canada

$84,100.00 - $113,700.00 · Full-time

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Job details

Pay: $84,100.00 - $113,700.00
Job type: Full-time
Posting language: English
Posted: Oct 19, 2026

Original job description

Job Description Summary

Are you a Quality Engineer experienced in risk-based validation within cGMP environments? Join our team to support processes, analytical methods, and equipment lifecycle verification.

In this role, you will be responsible for generating and supporting higher level project documentation, such as master plans, schedules, risk assessments, protocols, and summary reports. This is a highly collaborative position, and you will work on the full range of project phase execution, including commissioning, qualification, validation, and project hand-over activities, within a variety of departments (e.g. Manufacturing, Quality Control, Process Development, and Instrumentation). This is your chance to work alongside motivated and intelligent individuals who are passionate about the work they do to support life science research.

Job Description

Duties and Responsibilities

Responsible for the development of metrics that report on the effectiveness of processes, status of improvement opportunities and progress against performance objectives to drive continuous improvement
Participate in the Process Performance Qualification (PPQ) conformance lot manufacturing that includes increased testing to demonstrate acceptability of the developed formulation and process; perform non-conformance and CAPA investigations as needed
Prepare, review and/or coordinate the execution of validation, commissioning and qualification documentation
Ensure appropriate procedures, processes and policies are established and implemented for quality assurance activities to assure compliance with applicable medical device and/or biopharmaceutical regulations and products
Educate, train, advise and coach other employees to ensure adherence to all applicable quality standards for assigned areas

Knowledge and Qualifications

Bachelor’s Degree in Biomedical Engineering or equivalent, in combination with suitable experience (2-6 years) in a validation job and familiarity with risk management (ISO 14971 and cGMP are an asset)
Experience in utilities, facilities, and equipment qualification (Manufacturing, Quality Control Lab, Controlled Temperature Chambers mapping and monitoring), as well as software assurance
Excellent technical report writing and strong ability to understand and analyze technical documents
Familiar with Continued Monitoring and Improvement concepts
Strong project management and time management skills, with professional certifications such as ISPE Membership, Project Management, ASQ/Six Sigma Certification or equivalence is an asset

#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:

$84,100.00 - $113,700.00

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 Quality Engineer will manage risk-based validation processes, including equipment lifecycle verification and the generation of master plans and protocols. They will also lead continuous improvement initiatives, perform CAPA investigations, and provide training to ensure adherence to quality standards.

Requirements

Candidates must hold a Bachelor’s degree in Biomedical Engineering or a related field with 2-6 years of experience in validation. Proficiency in cGMP, risk management, and technical documentation is essential for this role.

Skills

Validation
cGMP
Risk management
Technical report writing
Project management
Quality assurance
CAPA
Process performance qualification
Equipment qualification
Software assurance
ISO 14971
Continuous improvement
Biotechnology
Instrumentation
Analytical methods

Benefits

Health benefits
Retirement savings
Career development opportunities

Visa sponsorship

Not detected in the job text

Keywords

Quality Engineer
Validation
cGMP
Risk management
ISO 14971
Biomedical Engineering
CAPA
PPQ
Quality assurance
Biopharmaceutical
Medical device
ISPE
ASQ
Six Sigma
ISO 14001
Biotechnology
Manufacturing
Quality control
Process development
Instrumentation
Software assurance
Technical writing
Project management
Life science research

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