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.

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.

• 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.