OmniaBio: Manufacturing Associate II

Hamilton, ON
On-site
Posted Sep 12, 2026
1 position

$65,000–$75,000 / year

Opens an external site

Employment type: Full-time
Experience level: Mid-level · 2+ years
Minimum education: College diploma
Posting language: English
Working hours: 40 hours per week

Job summary

The Manufacturing Associate II executes production processes for cell and gene therapies while adhering to GMP standards and documentation practices. They are responsible for operating clean room equipment, maintaining safety standards, and participating in root cause investigations.

Job details

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 a Manufacturing Associate II at OmniaBio, you will be experienced in biologics manufacturing. The person in this role will be part of a high-performing team focused on production projects adhering to Good Manufacturing Practices (GMP) at OmniaBio’s Hamilton, 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 of OmniaBio’s client service provision to manufacture life-saving cell and gene therapies Responsibilities: Follows OmniaBio’s policies, standard operating procedures and GMP documentation, adhering to Good Documentation Practice. Utilizes aseptic techniques and behaviours in the execution of the production process. Operates and cleans clean room equipment. 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 is maintained in 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 root cause of non-conformance activities. Adopts the OmniaBio Operating Model and embraces a continuous improvement approach to all work activities. Engages in training and development to take on increased responsibility. Provides guidance and support to less experienced colleagues within the Manufacturing team. Helps drive standards to ensure a successful work environment. Utilizes the SAP enterprise resource planning system to support manufacturing activities. Qualifications and experience: Two-year college program plus two years minimum of relevant experience. GMP and cleanroom experience. Strong English written and verbal communication skills. Able to lift or carry up to 20 pounds. Desired Competencies and Behaviors: Able to learn. Possesses integrity. Demonstrates resilience and tenacity. Diligent. Able to work in a team. Demonstrates interpersonal awareness. High-energy. 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.

What you’ll do

Requirements

Candidates must have a two-year college program and at least two years of relevant experience in biologics manufacturing. Proficiency in GMP, cleanroom environments, and strong English communication skills are required.