Manufacturing Associate I (12-Month Contract)

OmniaBio Inc; Ontario; On-site; CAD 50,000 - 70,000; Full time

Job summary

OmniaBio Inc is seeking a Manufacturing Associate II to join their team in Hamilton, Ontario. This site-based role involves executing GMP-compliant manufacturing activities for life-saving cell and gene therapies, within a team dedicated to continuous improvement and safety standards.

Qualifications

• Two years minimum of relevant experience.
• GMP and cleanroom experience required.
• Able to lift or carry up to 20 pounds.

Responsibilities

• Execute manufacturing activities adhering to GMP.
• Operate and clean clean room equipment.
• Participate in investigations for non-conformance.

Skills

English communication

Aseptic techniques

Teamwork

Education

Two-year college program

Tools

SAP

Job description

Department: Operations

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.

Revision number: OBMFGAII-20240404