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Added 13 mins ago
Project Coordinator
Mawg Design
Toronto, ON
Full-time
At Mawg Design, we foster an environment where creative solutions and teamwork drive success. As a Project Coordinator, you’ll play an integral role in ensuring that our projects run…
Added 13 mins ago
Advanced Rental Delivery
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Whistler, BC
Temporary
This multi-faceted position requires employees who can work in a fast paced environment, keep to a tight delivery schedule, and work with minimal supervision. You will gain valuable skills…
Added 13 mins ago
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AB · Edmonton, AB
Full-time
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Added 14 mins ago
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Full-time
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Municipality of East Hants, Nova Scotia, Canada
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Added 3 hours ago
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Regina, SK
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$24 to $33 CAD / hour
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Vancouver, BC
$55,000 to $65,000 CAD / year
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Added 3 hours ago
Health & Safety and Fleet Coordinator
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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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