
Omnia Bio is a technology-focused, global cell and gene therapy CDMO that specializes in manufacturing gene-modified cell therapies and viral vectors. With a strong emphasis on automation and artificial intelligence within a Good Manufacturing Practices (GMP) environment, Omnia Bio offers comprehensive services from preclinical to commercial manufacturing. Strategically located in Hamilton, Ontario, and backed by over a decade of expertise from CCRM, the company is positioned to meet the surging global demand for cell and gene therapy manufacturing. Omnia Bio's focus on immune cell-based therapies, induced pluripotent stem cell therapies, and lentiviral vectors allows it to drive advancements in the field, ensuring that transformative treatments reach patients effectively.

Omnia Bio is a technology-focused, global cell and gene therapy CDMO that specializes in manufacturing gene-modified cell therapies and viral vectors. With a strong emphasis on automation and artificial intelligence within a Good Manufacturing Practices (GMP) environment, Omnia Bio offers comprehensive services from preclinical to commercial manufacturing. Strategically located in Hamilton, Ontario, and backed by over a decade of expertise from CCRM, the company is positioned to meet the surging global demand for cell and gene therapy manufacturing. Omnia Bio's focus on immune cell-based therapies, induced pluripotent stem cell therapies, and lentiviral vectors allows it to drive advancements in the field, ensuring that transformative treatments reach patients effectively.
Job Title : EM Laboratory Supervisor
Revision No.: OBQCEMLEAD-20241204
Department : Quality Control
Working Arrangement: On Site
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 Microbiology EM Supervisor at OmniaBio, you are an experienced leader in the field of Environmental Monitoring for Good Manufacturing Practices (GMP) manufacturing. The Microbiology EM team is responsible for all Environmental Monitoring and APS programs and all outputs associated with each. The Microbiology EM Supervisor, will be required to work specifically to maintain the environmental conditions in clean rooms by managing the EM program, through EM sample management, data management and trending and the APS program through sample management, visual inspection of media fills and growth promotion testing of media. The successful candidate will demonstrate flexibility within the quality team and larger organization, flowing to work priorities, as required. Environmental monitoring (EM) is an enabling function and, as such, this role will support production and facility needs to ensure product supply to patients. You will ensure the high-quality delivery of contract services.
Responsibilities:
Requirements:
Desired Characteristics:
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.