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Warehouse Associate - Loader/Unloader - 3rd Shift
Cintas
Toronto, ON
Cintas is seeking a Warehouse Associate – Loader/Unloader to support the Rental Division. Loader/Unloaders are responsible for driving company trucks to designated areas in the facility for…
Added 30 mins ago
AG
QA - Data Reviewer, Associate
AtomVie Global Radiopharma Inc.
Hamilton, ON
- Full-time
The QA – Data Reviewer, Associate is responsible for ensuring GMP compliance and data integrity through verification of records generated in sampling, preparation, instrumental analysis,…
Added 45 mins ago
VA
AMT SALES ASSOCIATE (Evening Shift)
Voyageur Aviation
North Bay, ON
- Full-time
As a key member of the Material Control team, the AMT Sales Associate (evening shift) will report to the Warehouse Manager, and will provide reliable, consistent, and knowledgeable support…
Added 1 hour ago
SS
Sales & Business Development Representative – Industrial Solutions
Shreem Systems & Solutions Pvt. Ltd
Brandon, MB
- Full-time
Requires three years of college or technical school resulting in an Associate’s degree or equivalent combination of education and related practical experience from local market.
Added 1 hour ago
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Associate Analyst - Inventory
EECOL
Red Deer, AB
- Full-time
As an Associate Analyst - Inventory you will be focused on inventory analysis and/or execution of strategies and processes to ensure that inventory and service levels are optimized.
Added 3 hours ago
Warehouse Associate - Distribution Centre
Sherwin-Williams
Barrie, ON
Have at least one (1) year of experience working in a manufacturing or distribution facility
Added 4 hours ago
SD
Genesis Program - Canada Services Associate Consultant
Siemens Digital Industries Software
Toronto, ON
- Full-time
Become a member of our Customer Outcome team as an Associate Consultants for our Genesis Program. Through this program, you will undergo 4 months of training that will provide you with the…
Added 6 hours ago
FA
Procurement / Indirect Sourcing Associate (Supply Chain)
FTAI Aviation
Montreal, QC
- Full-time
We are seeking a Procurement (Indirect Sourcing) Associate to join our growing Supply Chain team in the aerospace sector. This role is ideal for a professional with experience in strategic…
Added 8 hours ago
OE
Senior Sales Associate, Service
Otis Elevator Co.
AB
- Full-time
Otis is growing and we are recruiting a Senior Sales Associate, Service to cover Edmonton and Northern Alberta territory and reporting to the Senior Manager & GM. This is for an existing…
Added 9 hours ago
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Associate Field Service Technician
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NS · Dartmouth, Nova Scotia
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Added 12 hours ago
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Shipper-Receiver
Wolf Steel Ltd
Barrie, ON
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Must have a Valid Forklift License for consideration - please submit with resume** · Must have an existing forklift certification and be able to pass an internal training & testing program
Added 14 hours ago
WC
(CAN) Stock Unloader Associate
Walmart Canada
Pickering, ON
- Full-time
Position Summary...Working as a Stock Unloader Associate at Walmart Canada is an excellent opportunity to build hands‑on experience in a fast‑paced retail environment. In this role, you…
Added 14 hours ago
MI
Picker/ Packer & Inventory Associate
Marketing Impact Limited
Concord, ON
- Full-time
At Marketing Impact, we're looking for a dependable, detail-oriented Picker/Packer & Inventory Associate to join our Operations team. In this hands-on role, you'll help ensure customer…
Added 14 hours ago
WC
(CAN) Distribution Centre Team Associate - Quality Assurance II - 9 months contract , Part time - Mon, Tue, Thurs - 21:00 - 5:30
Walmart Canada
Mississauga, ON
- Part-time
- Contract
Added 14 hours ago
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Laboratory Assistant – Bioprocess Trainee – Bioprocess Development Group, Lallemand Inc.
Lallemand
Montreal, QC
- Full-time
…selected candidate will work under the guidance of the Operations Associate and will be responsible for, but not limited…
Added 15 hours ago
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Material Handler
Wolf Steel Ltd
Barrie, ON
- Full-time
Must have complete knowledge of all Material Handling practices
Added 15 hours ago
EI
Laboratory Technician, Chemical Manufacturing
Ecolab Inc.
Mississauga, ON
- Full-time
Experience working in a manufacturing lab environment
Added 15 hours ago
US
Early Morning Warehouse Associate
UPS Supply Chain Solutions
Ajax, ON · CA - AJAX BUILDING (ONAJX)
- Part-time
The Warehouse Associate’s position is a physical fast-paced and labor-intensive role within a warehouse environment that involves sorting/stocking packages as well as loading and unloading…
Added 16 hours ago
AT
Senior Associate, Quality Assurance & Regulatory Affairs
Adler Therapeutics
Toronto, ON · Greater Toronto Area, Canada
- Full-time
Adler Therapeutics Inc. is looking for a motivated and detail-oriented Senior Associate, Quality Assurance & Regulatory Affairs to join our growing team.
Added 16 hours ago
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Customer Success Associate - 12 Month Contract
Trudell Medical International
London, ON
- Contract
customer Success Associate - 12-Month Contract
Added 16 hours ago
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Associate Field Service Technician
ABB
Dartmouth, NS
- Full-time
Added 17 hours ago
US
Bypass Early Morning Warehouse Associate
UPS Supply Chain Solutions
Toronto, ON · CA - TORONTO HUB (ONTOR)
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The Warehouse Associate’s position is a physical fast-paced and labor-intensive role within a warehouse environment that involves sorting/stocking packages as well as loading and unloading…
Added 17 hours ago
W
(CAN) Distribution Centre Team Associate - Quality Assurance II - 9 months contract , Part time - Mon, Tue, Thurs - 21:00 - 5:30
Walmart
Mississauga, ON
- Part-time
Added 17 hours ago
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Material Handler
Napoleon
Barrie, ON
- Full-time
Must have complete knowledge of all Material Handling practices
Added 17 hours ago
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Quality Engineering Specialist
Syntronic
Ottawa, ON
- Full-time
Syntronic Production Services Canada is an Electronic Manufacturing Services provider located in Ottawa’s west end. Committed to our customers’ success, we understand that our people are…

CCRM and OmniaBio

OmniaBio: Quality Control Associate I

Hamilton, ON, Canada

Apply on jobs.dayforcehcm.com About employer

Applications open in a new tab.

Job details

Posting language: English
Posted: Sep 24, 2026

Original job description

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.

Active Vacancy

Position Summary:

As the Associate I, Quality Control at OmniaBio, you are a motivated individual with a keen interest in the field of quality control (QC) for Good Manufacturing Practices (GMP) manufacturing of cell and gene therapy products, driven by the opportunity to enable clinical translation of cell therapy and regenerative medicine. The Associate I, Quality Control, will be required to work across the entire range of activities, including but not limited to, testing, sample management, equipment qualification, method development and optimization, and data review. You will demonstrate flexibility within the Quality team and larger organization, managing work priorities, as required. You will ensure the high-quality delivery of contract services.

Responsibilities:

Delivers quality control-related services, including sample management, testing, method development, optimization, qualification and validation, stability program, data review and equipment management.

Complies with all standard operating procedures (SOPs) and work practices.

Maintains the materials specification program, as directed.

Releases materials, as directed.

Manages the retain and reference standard program, as directed.

Adheres to the QC documentation quality management system program, including SOPs, logbook and associated forms.

Maintains the sample management program, including sample identification, storage and retention.

Performs material testing in compliance with approved and current specifications, including but not limited to, incoming materials, in-process materials, drug substance materials, drug product materials, environmental monitoring samples, and stability samples, as required.

Participates in internal audits and/or supplier audits, as required.

Participates in client audits and health authority audits, as required.

Collaborates with the Facilities and Engineering team to ensure that facilities are available for production, including but not limited to, room readiness and environmental monitoring data.

Reviews and assesses deviations, corrective and preventative actions, change controls, etc.

Continuously grows and adapts in a fast-moving field to keep yourself and the organization at the forefront of the cell and gene therapy and regenerative medicine fields.

Ensures GMP is embedded in all manufacturing related tasks.

Engages and supports the OmniaBio Operating Model continuous improvement philosophy.

Requirements:

High school diploma, college diploma preferred.

1-2 years of experience in cell therapy/viral quality control department supporting GMP production, or similar within the pharmaceutical, medical technologies, biologics or similar industries.

Experience working for a CDMO, a third-party testing facility or a biotechnology company performing similar activities.

Strong understanding of cell manufacture processes and technologies.

Excellent understanding of Health Canada/US Food and Drug Administration GMP regulations and quality assurance principles.

Desired Characteristics:

Sound knowledge of applicable regulatory frameworks and requirements for cell and gene therapy and regenerative medicine, such as GMP, ISO, or medical device development.

Independent, detail-oriented self-starter with excellent analytical skills and able to multitask and succeed in a team environment.

Experience establishing customer-facing organizations and service models.

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.

Apply on jobs.dayforcehcm.com About employer

More about this job

Responsibilities

The Quality Control Associate I is responsible for performing material testing, sample management, and equipment qualification in compliance with GMP standards. They also participate in internal and external audits while ensuring all documentation and quality management systems are maintained.

Requirements

Candidates must have a high school diploma, with a college diploma preferred, and 1-2 years of experience in a cell therapy or viral quality control department. A strong understanding of GMP regulations and cell manufacturing processes is required.

Skills

Quality Control
GMP
Cell Therapy
Gene Therapy
Sample Management
Equipment Qualification
Method Development
Data Review
Environmental Monitoring
Regulatory Compliance
Standard Operating Procedures
Material Testing
Auditing
Documentation
Biomanufacturing
Analytical Skills

Visa sponsorship

Not detected in the job text

Keywords

Quality Control
GMP
Cell Therapy
Gene Therapy
CDMO
Regenerative Medicine
Biomanufacturing
SOP
Environmental Monitoring
Health Canada
FDA
Quality Assurance
Validation
Stability Program
Deviations
Corrective and Preventative Actions
Change Controls
Lentiviral Vectors
Automation
Robotics
Artificial Intelligence
Documentation
Auditing
Material Specification
Sample Management
Equipment Management
Clinical Translation
Biologics
Pharmaceutical

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Jobs in Canada