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.