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Added 13 mins ago
RPA UiPath developer
K&K Global Talent Solutions INC.
Toronto, ON
$110,000 to $115,000 CAD / year
Full-time
Integrate automation with APIs, databases, and third‐party applications as required.
Added 15 mins ago
Full-Stack Developer
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Full-time
CI/CD pipelines, Docker, Kubernetes, and infrastructure automation
Added 30 mins ago
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2+ years of experience working on enterprise SaaS, workflow, platform, data, AI, automation, or developer/productivity tools.
Added 44 mins ago
QE Delivery Manager – Quality Engineering & Automation
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ON · Ontario, Canada
Full-time
Position: QE Delivery Manager – Quality Engineering & Automation
Added 44 mins ago
Software Engineer in Test
Randstad Digital
Toronto, ON
Contract
…contract. In this role, you will lead test planning, build automation frameworks, and execute comprehensive test suites to ensure our applications meet functional, non-functional, and…
Added 1 hour ago
Business Analyst – KYC / Fraud & AML
Staffingine LLC
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Identify process gaps, risks, and opportunities for automation and process optimization.
Added 1 hour ago
Application Development Supervisor - Systems Analysis Unit Supervisor
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Four (4) years of progressive work experience in supporting an open-source developer platform, such as .NET Technologies.
Added 1 hour ago
Business Systems - Test Automation Lead
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Build and lead a pragmatic test automation and performance assurance program that improves the reliability of enterprise systems while reducing the cost and effort of repetitive testing.…
Added 2 hours ago
Junior QA Automation Engineer
Robert Half
Toronto, ON · North York, ON
Contract
We are looking for a Junior QA Automation Engineer to join a technology team in North York, Ontario. This opportunity is ideal for an early-career quality assurance professional who is…
Added 2 hours ago
Senior QA Engineer
Questrade Financial Group
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Added 6 hours ago
Senior Guidewire QA Engineer
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$60,000 to $90,000 CAD / year
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Must have hands on automation knowledge, BDD Cucumber.
Added 9 hours ago
Senior Business Analyst (KYC)
Altimetrik
Mississauga, ON
Full-time
Identify process gaps, risks, and opportunities for automation and optimization.
Added 9 hours ago
Lead QA Engineer
Royal Bank of Canada
Toronto, ON
Full-time
We are looking for a highly experienced Quality Engineering (QE) Lead to drive Quality Engineering practices and test automation excellence for Emerging Payments application within RBC…
Added 11 hours ago
Software Test Developer Assistant Vice President
Citi
Mississauga, ON
Full-time
We are looking for a hard-working, and driven Automation QA Engineer to become a valuable addition to our team. The perfect fit is someone who enjoys challenges, navigates ambiguity, and…
Added 11 hours ago
Senior Full Stack Developer – Java / Angular
Tata Consultancy Services
Toronto, ON
$90,000 to $110,000 CAD / year
Full-time
We are seeking a Senior Full Stack Developer with leadership skills to join a high-performing engineering team building modern, customer-facing web applications and resilient backend…
Added 11 hours ago
QE Automation
Tata Consultancy Services
Toronto, ON
$90,000 to $110,000 CAD / year
Full-time
Quality Engineering and Test Automation experience.
Added 13 hours ago
Quality Control Coordinator
OmniaBio
Hamilton, ON
$55,000 to $65,000 CAD / year
Contract
…therapies, with a mission to transform biomanufacturing with AI and automation. Located at McMaster Innovation Park in Hamilton, Ontario, OmniaBio leverages over a decade of expertise in…
Added 13 hours ago
OmniaBio: Quality Control Coordinator (12-month contract)
CCRM and OmniaBio
Hamilton, ON
…therapies, with a mission to transform biomanufacturing with AI and automation. Located at McMaster Innovation Park in Hamilton, Ontario, OmniaBio leverages over a decade of expertise in…
Added 15 hours ago
Project Coordinator
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$70,000 to $80,000 CAD / year
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Technical knowledge of electrical, mechanical, HVAC, refrigeration, or building automation and controls
Added 15 hours ago
KYC Business Analyst
W3Global
Mississauga, ON
$100,000 to $115,000 CAD / year
Full-time
Identify process gaps, risks, and opportunities for automation and optimization.
Added 16 hours ago
Marketing Operations Coordinator
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Full-time
Added 16 hours ago
Ingénieur QA en automatisation
Amaris Consulting | Part of Mantu
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Full-time
You will be supporting different projects through your expertise as QA Automation Engineer.
Added 17 hours ago
Business Analyst – KYC / Fraud & AML
Staffingine LLC
Mississauga, ON
Full-time
Identify process gaps, risks, and opportunities for automation and process optimization.
Added 17 hours ago
Business Analyst with Fraud/AML
Talenzaa
Mississauga, ON
Full-time
Identify process gaps, risks, and opportunities for automation and optimization.
Added 18 hours ago
Senior Python Developer
Collabera
Toronto, ON
$80 to $90 CAD / hour
Contract
We are seeking an experienced Python Developer to join a high-performing Equity Linked Technology team responsible for building innovative pre-trade solutions for Equity Derivatives…

OmniaBio

Quality Control Coordinator

Hamilton, ON, Canada

Pay: $55,000 to $65,000 CAD / year
Job type: Contract
Apply by: Oct 24, 2026
Experience: Up to and including 1 year of practical and related experience and/or 6 months on-the-job training in pharmaceutical, medical technologies, biologics or similar industries.
Posting language: English
Posted: Sep 24, 2026

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Original job description

Active Vacancy

About OmniaBio:

OmniaBio Inc. is a technology-driven, global CDMO specializing in cell and gene therapies, with a mission to transform biomanufacturing with AI and automation. Located at McMaster Innovation Park in Hamilton, Ontario, OmniaBio leverages over a decade of expertise in regenerative medicine and advanced therapies developed in partnership with CCRM. Committed to digital transformation, OmniaBio integrates automation, robotics, and artificial intelligence into its operations to drive efficiency, enhance quality, and increase throughput. This innovative approach supports end-to-end CDMO services - from development through GMP manufacturing and scale-up - helping clients accelerate the path to market for transformative treatments. OmniaBio focuses on immune cell-based therapies, induced pluripotent stem cell therapies, and lentiviral vectors, positioning itself as a leader in advancing and maturing cell and gene therapy manufacturing. With a strategic vision to meet the surging global demand, OmniaBio aims to enable broad access to cutting-edge therapies worldwide.

Visit www.omniabio.com to learn more.

Position Summary:

As the Quality Control Coordinator at OmniaBio, you are a motivated individual in the field of Quality Control for Good Manufacturing Practices (GMP) manufacturing. The Quality Control (QC) team is responsible for all aspect of QC for the organization and the Quality Control Coordinator will be required to work across the entire range of activities, including but not limited to materials management, sample management, data review and compliance activities. You will demonstrate flexibility within the quality and larger organization, following the work priorities as required. You will provide support to ensure the department activities are completed on time and as assigned. You will ensure the high-quality delivery of contract services.

Responsibilities:

Deliver quality control related services as contracted, to various cell and viral product centered clients.
Comply with all standard operating procedures and work practices.
Manage retain and reference standard program as directed.
Maintain the sample management program, including sample identification, storage and retention.
Maintain QC materials management program, including inventory management, ordering and receipt.
Assist with QC doc control and compliance management.
Assist with data review of QC test records and log books as required.
Participate in internal audits and/or supplier audits as required.
Participate in Client audits and Health Authority audits as required.
Continuously grow and adapt in a fast-moving field to keep yourself and the organization at the forefront of the cell and gene therapy and regenerative medicine fields.
Engage and support the OmniaBio Operating Model (OBOM) CI philosophy
Adhere to the QC documentation (QMS) program, including SOPs, logbooks and associated forms.
Work with QA, Production, SC and MSAT colleagues to remedy non-compliance and adherence to Good Documentation Practices.
Support in coordinating the third-party testing by OmniaBio approved laboratories.
Continuously grow and adapt in a fast-moving field to keep yourself and the organization at the forefront of the cell and gene therapy regenerative medicine fields.
As required, any other related activities in the Quality Control Department.

Requirements:

Highschool + additional science related program up to 1 year.
Up to and including 1 year of practical and related experience and/or 6 months on-the-job training in pharmaceutical, medical technologies, biologics or similar industries.
Flexible to work in the fast-paced working environment.

Desired Characteristics:

Independent, detail-oriented, self-starter with the ability to multitask and succeed in a team environment.
Demonstrated initiative and the ability to deliver high quality outcomes.

OmniaBio is a developing organization and represents a fluid working environment. Flexibility and adaptability are essential, and duties will be influenced by the needs of the organization.

Applicants must be legally eligible to work in Canada.

An applicant’s compensation package is finalized once the interview process is concluded and accounts for the nature of the role as well as the experience, competencies (job knowledge, skills and abilities) of the applicant and internal equity.

OmniaBio is committed to accessibility, diversity, and equal opportunity. Requests for accommodation can be made at any stage of the recruitment process, providing the applicant has met the bona fide requirements for the open position. Applicants should make their requirements known once contacted to schedule an interview, or when the job offer has been made.

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More about this job

Responsibilities

Coordinate QC activities for cell and viral therapy clients, including sample and materials management, retain and reference standards, documentation, data review, and third-party testing. Follow GMP and QMS procedures, support audits and compliance improvements, and collaborate with QA, Production, Supply Chain, and MSAT teams.

Requirements

Requires a high school education plus an additional science-related program of up to one year. Requires up to one year of relevant practical experience or six months of on-the-job training in pharmaceutical, medical technology, biologics, or a similar industry, along with flexibility in a fast-paced environment.

Skills

Quality Control
GMP Compliance
Sample Management
Materials Management
Inventory Management
Data Review
Document Control
Good Documentation Practices
Audit Support
Third-Party Laboratory Coordination
Attention To Detail
Multitasking
Adaptability
Continuous Improvement
Teamwork

Visa sponsorship

Not detected in the job text

Keywords

Quality Control
Good Manufacturing Practices
Cell And Gene Therapy
Regenerative Medicine
Biologics
Pharmaceutical Manufacturing
GMP Manufacturing
Quality Management System
Standard Operating Procedures
Good Documentation Practices
Sample Management
Materials Management
Inventory Management
Retain Samples
Reference Standards
Data Review
QC Test Records
Logbooks
Document Control
Compliance Management
Internal Audits
Supplier Audits
Client Audits
Health Authority Audits
Third-Party Testing
Approved Laboratories
Continuous Improvement
Automation
Robotics
Artificial Intelligence

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