OmniaBio: Manufacturing Associate I (Permanent/Contract
Listed on 2026-08-04
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Manufacturing / Production
Production Associate / Production Line, Pharmaceutical Manufacturing, Manufacturing Engineer, Manufacturing & Industrial Operations
Omnia Bio:
Manufacturing Associate I (Permanent/Contract)
Hamilton, ON, Canada
Job DescriptionPosted Friday, July 31, 2026 at 4:00 AM
About Omnia Bio:
Omnia Bio 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, Omnia Bio leverages over a decade of expertise in regenerative medicine and advanced therapies developed in partnership with CCRM. Committed to digital transformation, Omnia Bio 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. Omnia Bio 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, Omnia Bio aims to enable broad access to cutting‑edge therapies worldwide.
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Active Vacancy
Position Summary:As a Manufacturing Associate Iat Omnia Bio, you will be part of a high‑performing team focused on production projects adhering to Good Manufacturing Practices (GMP) atOmnia
Bio’sHamilton, Ontario, facility.
This position is site‑based, with work hours adhering to a designated pattern of 12‑hour shifts.
The primary function of this role is to execute manufacturing activities in support ofOmnia
Bio’sclient service provision to manufacture lifesaving cell and gene therapies.
- Follows Omnia Bio ’spolicies, standard operatingproceduresand GMP documentation, adhering to Good Documentation Practice.
- Utilizes aseptic techniques andbehavioursin the execution of the production process under the guidance of experienced colleagues and management.
- Operates and cleans cleanroom equipment.
- UtilizeSAPenterprise system for supporting manufacturing activities.
- Supports room and equipment commissioning, qualification and validation activities associated with enabling GMP operations and the introduction of new manufacturing processes.
- Ensures that classified space within the manufacturing area ismaintainedin a clean and safe state of control.
- Responsible for the health and safety of the individual, co‑workers, and visitors to the manufacturing area.
- Participates in investigations to derive rootcauseof non‑conformance activities.
- Adopts the Omnia Bio Operating Model and embraces a continuous improvement approach to all work activities.
- Engages in training and development to perform work in GMP clean rooms and take on increased responsibilities.
- High School Diploma or a higher qualification
- Experience with in a manufacturing environmentutilizingdocumented procedures would be preferable.
- Strong English written and verbal communication skills.
- Experience in a working environment
- Able to lift or carry up to 20 pounds.
- Able to learn.
- Possesses integrity.
- Demonstrates resilience and tenacity.
- Able to work in a team.
- Demonstrates inter‑personal awareness.
- High‑energy.
Omnia Bio 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.
Omnia Bio 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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