OmniaBio: Manufacturing Associate I (12-month Contract)

OmniaBio Inc.; Hamilton; Hybrid; CAD 52,000 - 66,000; Full time

Job summary

OmniaBio Inc. in Hamilton, Ontario, is seeking a Manufacturing Associate I to join a GMP-focused production team within a cleanroom environment. The role is site-based with 12-hour shifts and a strong emphasis on safety, quality, and documentation.

You will execute manufacturing activities, operate equipment, support commissioning and validation, and collaborate with colleagues to deliver reliable client services for cell and gene therapies.

Qualifications

• High School Diploma or higher.
• Experience in manufacturing with documented procedures preferred.
• Strong English written and verbal communication skills.
• Able to lift or carry up to 20 pounds.

Responsibilities

• Follow GMP policies, SOPs, and GMP documentation.
• Utilize aseptic techniques under supervision.
• Operate and clean cleanroom equipment.
• Utilize SAP for supporting manufacturing activities.
• Support commissioning, qualification and validation activities.
• Maintain clean and safe space within manufacturing area.
• Ensure health and safety of personnel in the area.
• Participate in investigations to derive root causes of non-conformance.
• Adopt OmniaBio Operating Model and pursue continuous improvement.
• Engage in training to perform GMP work in cleanrooms.

Skills

English skills

Teamwork

Learning agility

Integrity

Resilience

Diligence

Education

High School Diploma or higher

Tools

SAP

Job description

Active Vacancy

Position Summary

As a ManufacturingAssociate Iat OmniaBio, you will be part of a high-performing team focused on production projects adhering to Good Manufacturing Practices (GMP) atOmniaBio’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 ofOmniaBio’sclient service provision to manufacture lifesaving cell and gene therapies.

Responsibilities

• FollowsOmniaBio’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.
• Ensuresthat 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 OmniaBio Operating Model and embraces a continuous improvement approach to all work activities.
• Engages in training and development to perform work in GMP cleanrooms and take on increased responsibilities.

Qualifications and experience

• High School Diploma or a higher qualification
• Experience within 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.

Desired Competencies and Behaviors

• Able to learn.
• Possesses integrity.
• Demonstrates resilience and tenacity.
• Diligent
• Able to work in a team.
• Demonstratesinter-personalawareness.
• High-energy.