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Added 3 mins ago
ES
Project Manager - Construction and Energy Efficiency at Toronto!
Equans Services Canada & US
Toronto, ON
- Full-time
Conduct quality assurance and quality control activities, including document reviews, approvals,
Added 3 mins ago
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EHS Manager
Veolia | Water Tech
Oakville, ON
- Full-time
Analyze data to proactively assess health and safety challenges, and to develop approaches to control risks; monitor and document EHS activities and corrective action plans to completion
Added 3 mins ago
V|
EHS Manager
Veolia | North America
Oakville, ON
- Full-time
Analyze data to proactively assess health and safety challenges, and to develop approaches to control risks; monitor and document EHS activities and corrective action plans to completion
Added 5 mins ago
FC
Customer Journey Optimization Developer
Fidelity Canada
Toronto, ON
- Full-time
Configure tracking, reporting inputs, A/B tests, holdouts, variants, and control logic required to measure journey performance
Added 5 mins ago
VC
Project Coordinator
Valard Construction
Calgary, AB
- Full-time
Review and distribute engineering drawings, design changes, and technical specifications to field teams, confirming that the latest document revisions are being always used on site
Added 20 mins ago
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Proposal Coordinator
EllisDon
Ottawa, ON
- Full-time
Manage document control and final production for all proposal response requirements.
Added 33 mins ago
HO
Millwright
Honda of Canada Mfg.
Alliston, ON
- Full-time
Document daily activities: equipment changes, downtime calls, work orders (WO), investigations, and CM results
Added 33 mins ago
HO
Industrial Electrician
Honda of Canada Mfg.
Alliston, ON
- Full-time
Document daily activities: equipment changes, downtime calls, work orders (WO), investigations, and CM results
Added 33 mins ago
VC
Executive Assistant - VP
VON Canada
ON · Ontario, Canada
- $30.9 to $32.83 CAD / hour
- Part-time
Develop and document processes to support teams and functions.
Added 33 mins ago
T
Senior ETL Developer – Azure, AWS & Databricks
ThoughtStorm
Toronto, ON
- Contract
Use Git and source control strategies while following software development lifecycle practices, including development, testing, QA, and delivery.
Added 33 mins ago
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Junior project management
Dexian
Montreal, QC · Greater Montreal Metropolitan Area
- $35 to $40 CAD / hour
- Contract
Apply PMO standards, quality expectations, and document-control practices consistently.
Added 35 mins ago
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Test Automation Engineer (Python / Playwright / D365)
PLATO
Calgary, AB · BC · Vancouver, BC · Winnipeg, MB · Fredericton, NB · Halifax, NS · Ottawa, ON · Sault Ste. Marie, ON · Toronto, ON · Gatineau, QC · Prince Albert, SK · Regina, SK
- Full-time
Execute automated and manual test activities and document test results, defects, and supporting evidence.
Added 50 mins ago
B
Field Operations Specialist
BinSentry
Kitchener, ON
- Full-time
…installation, configuration, data quality, and operating conditions. Document findings, track next steps, and escalate issues to the appropriate teams for…
Added 50 mins ago
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Construction Site Administrator
FRAM + Slokker
Peterborough, ON
- Full-time
Added 50 mins ago
HP
327-26 Registered Respiratory Therapist, Cardiorespiratory (Outpatient Clinic), Regular Part-time, Alliance Wide
Huron Perth Healthcare Alliance
Stratford, ON
- Part-time
…and the hospital, including adherence to all HPHA infection control procedures, including hand hygiene procedures and Personal Protective Equipment as…
Added 50 mins ago
HP
352-26 Environmental Services I, Full-Time, Stratford
Huron Perth Healthcare Alliance
Stratford, ON
- Full-time
…methodologies, as well as having the ability to apply infection control standards. Housekeeping can be performed in patient rooms, nursing stations, hallways, bathrooms, offices, and other…
Added 50 mins ago
T
Senior Finance Analyst
TD
Toronto, ON
- Full-time
Identify, document, investigate processes / exceptions arising from transactions / processes beyond 1st level operations service delivery and resolve escalated matters and refer complex…
Added 50 mins ago
BC
Project Coordinator - Buildings East
Bird Construction
Winnipeg, MB
- Full-time
Organizes and maintains project site files and documentation, including electronic document management systems and shared file platforms
Added 54 mins ago
FF
Quality assurance (qa) technician
Fresh forward Inc.
Edmonton, AB
- $17 to $19 CAD / hour
- Full-time
- On-site
Document and report deviations from specifications and tolerances
Added 1 hour ago
SH
Part Time - Kinesiologist or Exercise Physiologist
Stem Health
Toronto, ON
- Part-time
Maintain Cosmed equipment calibration, quality control procedures, and testing environment standards to ensure reproducible, clinically reliable results across all assessments.
Added 1 hour ago
GT
Electric Utilities OCM Consultant (ADMS)
Grid Transformation
Canada
- Full-time
…System (OMS), Distribution Management System (DMS), Supervisory Control and Data Acquisition (SCADA), Advanced Metering Infrastructure (AMI), Distributed Energy Resource Management System…
Added 1 hour ago
GT
ADMS Test Manager
Grid Transformation
Canada
- Full-time
…System (OMS), Distribution Management System (DMS), Supervisory Control and Data Acquisition (SCADA), Advanced Metering Infrastructure (AMI), Distributed Energy Resource Management System…
Added 1 hour ago
DH
Quality Assurance/ Quality Control Inspector - Mid Canada Mod Centre
De Havilland Aircraft of Canada Limited
Breslau, ON
- Full-time
The QA/QC Inspector (Manufacturing) supports Manufacturing operations by performing Quality Control (QC) inspection functions within the Manufacturing system and Quality Assurance (QA)…
Added 1 hour ago
AG
Vice President of Quality
AtomVie Global Radiopharma Inc.
Hamilton, ON
- Full-time
…schedules, the position oversees the Quality Assurance, Quality Control, Sterility Assurance, Validation, and Analytical Development functions. The position also provides leadership and…
Added 1 hour ago
BP
Document Control and Proposal Coordinator
Bunch Projects
Calgary, AB
- Full-time
We are seeking an experienced Document Control and Proposal Coordinator to support the full lifecycle delivery of EPC projects and contribute to the overall efficiency of our operations.

Aspect Biosystems

Quality Assurance Specialist

Vancouver, BC, Canada

The hiring range for this role is $73,863 - $92,329, annually.

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Job details

Pay: The hiring range for this role is $73,863 - $92,329, annually.
Posting language: English
Posted: Oct 1, 2026

Original job description

We are seeking a Quality Assurance Specialist to strengthen and oversee our quality assurance development. You will pioneer and execute quality assurance activities associated with clinical Good Manufacturing Practices (GMP) of our bioprinted cell therapies. With a passion for optimization, you will also drive continuous improvement of our manufacturing and quality systems by developing, applying, revising, and maintaining quality metrics.

Responsibilities

Support in development of internal QA processes and procedures and implementation of the company’s Quality Management System (QMS).
Maintain and provide document control support.
Assist in development of training content for QA processes, maintain training and certification requirements for the position.
Identify and evaluate issues and/or gaps in processes and documentation and propose effective solutions to remediate.
Provide QA expertise on change management, and support implementation of documents, design, process, and material related changes.
Collaborate closely with R&D teams from the early development phases to embed quality standards directly into product designs, technical documentation, and underlying engineering processes
Support the internal vendor qualification program by ensuring vendor documents are up to date and compliant.
Be the quality assurance and documentation expert and support cross-functional groups on:

Reviewing study protocols and reports
Creating, reviewing, approving, and implementing SOPs, Policies, forms, and other controlled documents
Reviewing data for completeness
Completing root cause analysis/ investigations and implementing appropriate corrective and preventive actions.

Review executed batch records to ensure compliance with Good Documentation practices and procedures; communicate and resolve discrepancies with the cross-functional teams.
Collaborate routinely with the CMC and QC teams during processing, bioprinting and testing, ensuring buy-in and ownership of our quality program.
Assist in the development of critical raw material specifications and review and approve incoming raw materials.
Support in the development and implementation of critical CMC equipment qualification.
Assist in Risk Management by conducting risk assessments on core raw materials.
Other duties as assigned.

Qualifications & Experience

Education & Experience: You hold a Bachelor's degree or Master’s degree in Biology, Biotechnology or another relevant discipline and 5-7+ years of hands-on experience developing, or administrating GMP quality programs in biotech, medical device, or pharmaceutical environments.
Regulatory Expertise: Demonstrated knowledge and application of industrial regulations including those of FDA, EMEA, and other authorities related to Biologics and/or Pharmaceuticals. Experience with medical device regulations is a plus.
Detail-Oriented: You have outstanding attention to detail as well as process rigour. You take pride in your work and strive for excellence.
Go-Getter: You work with a sense of urgency, are results-driven, and thrive in a fast-paced, interdisciplinary, and entrepreneurial environment. You are willing to roll up your sleeves and do what it takes to get the job done.
Collaborative: You thrive in a multi-disciplinary team environment and believe that we can get further, faster by working together.

The hiring range for this role is $73,863 - $92,329, annually. Our ranges are based on market data. Offered salaries will be based on a combination of factors including, but not limited to, job-related knowledge, skills, education, and experience. For candidates who exceed role requirements, we are open to exploring above-range offers. Note that base salary is just one part of the overall compensation at Aspect. Members of the Aspect team also receive equity, a comprehensive benefits package, and support for continuous learning and career progression.

Who We Are

Aspect Biosystems is a biotechnology company pioneering the development of a novel category of regenerative medicine designed to restore or supplement biological function and deliver curative therapies for some of the most elusive diseases. Aspect is developing these bioengineered cellular medicines by applying its full-stack tissue therapeutic platform, which integrates proprietary AI-powered bioprinting technology, therapeutic cells, hypoimmune cell engineering, and advanced biomaterials. Aspect is advancing its therapeutic pipeline across multiple endocrine and metabolic diseases, including diabetes and rare endocrine disorders. If you are committed to making a real impact and accelerating the development of life-changing therapies, we want to hear from you!

Curious about our current perks and benefits? Learn more here.

At Aspect Biosystems, our strength has always been in our diversity. Different people, thinking differently, unified in creating a world that is better for us all. We are committed to creating an inclusive environment for everyone on our team.

All aspects of employment - including the decision to hire, promote, discipline, or terminate - are based on merit, competence, performance, and business needs. We do not discriminate on the basis of race, color, religion, citizenship status, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, political affiliation, or any other status protected under federal, state, provincial, or local law.

If you're interested in joining our team but don't see a job posting that matches your experience or background, we encourage you to submit a general application to be considered for future opportunities!

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More about this job

Responsibilities

The Quality Assurance Specialist will oversee and execute quality assurance activities for bioprinted cell therapies in compliance with GMP standards. They will also drive continuous improvement of manufacturing and quality systems by developing metrics, managing documentation, and collaborating with cross-functional teams.

Requirements

Candidates must hold a Bachelor's or Master's degree in Biology, Biotechnology, or a related field. They are required to have 5-7+ years of hands-on experience in GMP quality programs within biotech, medical device, or pharmaceutical environments.

Skills

Quality Assurance
GMP
Quality Management System
Document Control
Regulatory Compliance
FDA
EMEA
Biologics
Pharmaceuticals
Root Cause Analysis
Corrective and Preventive Actions
Risk Management
SOP Development
Batch Record Review
Vendor Qualification
CMC

Benefits

Equity
Continuous learning support
Career progression support

Visa sponsorship

Not detected in the job text

Keywords

Quality Assurance
GMP
Bioprinting
Cell Therapies
QMS
Document Control
FDA
EMEA
Biologics
Pharmaceuticals
Medical Device
SOP
Root Cause Analysis
CAPA
Batch Records
CMC
QC
Risk Management
Raw Materials
Biotechnology
Regenerative Medicine
AI-powered
Tissue Engineering
Compliance
Process Rigour
Change Management
Vendor Qualification
Technical Documentation
Engineering Processes
Quality Metrics

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