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Manufacturing Support Technician (12-Month Contract)

OmniaBio

Hamilton

On-site

CAD 40,000 - 55,000

Full time

4 days ago
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Job summary

OmniaBio is seeking a Manufacturing Support Technician in Hamilton, Ontario. This site-based position involves working in a clean room environment supporting the production of cell and gene therapies by ensuring material integrity and adhering to GMP practices. Extensive training will be provided, making this an excellent entry-level opportunity for candidates looking to start their career in a high-demand field.

Qualifications

  • Entry-level position; high school diploma or higher required.
  • Experience in a manufacturing environment preferred.
  • Strong English communication skills.

Responsibilities

  • Support clean room manufacturing activities and maintain cleanliness.
  • Utilize SAP system for manufacturing activities.
  • Adhere to Good Manufacturing Practices (GMP) and safety regulations.

Skills

Communication
Teamwork
Diligence

Education

High school diploma or higher qualification

Tools

SAP

Job description

JobTitle:ManufacturingSupport Technician
Department:OmniaBio Operations
PositionSummary:
As a Manufacturing Support Technician at OmniaBio,you willbe part of a high-performing team focused on production projects adhering to Good Manufacturing Practices (GMP).This role is site-based, and involves working regularly scheduled 12-hour shifts at OmniaBio’s Hamilton, Ontario, facility. The primary purpose of this role is to support clean room manufacturing activities by facilitating material supply and removal of waste. This is an entry-level position, but plays an important role in supporting OmniaBio’s client service provision to manufacture life-saving cell and gene therapies. Extensive training will be provided at the Canadian Advanced Therapies Training Institute training site at the University of Guelph, in partnership with OmniaBio.
Responsibilities:
  • Follows OmniaBio’s policies, standard operatingprocedures and GMP documentation, adhering to GoodDocumentation Practice.
  • Ensures the integrity of materials and supplies in delivery to clean rooms are not compromised.
  • Removes waste, adhering to strict procedures to prevent cross-contamination.
  • Maintainscleanliness of production support areas and equipment employed under control of the job holder.
  • Utilizes the SAP enterprise resource planning system to support manufacturing activities.
  • Ensures that classified space within the manufacturing area is maintained in a clean and safe state of control.
  • Ensures the health and safety of the individual, co-workers and visitors to the manufacturing area.
  • Adopts the OmniaBio Operating Model (OBOM) and embraces a continuous improvement approach to all work activities.
  • Engages in training and development to perform work in GMP clean rooms and takes on increased responsibilities.
  • Liaises with clean room manufacturing personnel and the Supply Chain and Quality Control teams to coordinate requirements in support of the batch manufacturing process.
Qualifications and experience:
  • High school diplomaor a higher qualification.
  • Experience within a manufacturing environment utilizing documented procedures is preferable.
  • StrongEnglishwrittenandverbalcommunicationskills.
  • Prior experience in a working environment.
  • Able toliftor carry upto20 pounds.
DesiredCompetencies and Behaviors:
  • Able to learn
  • Possesses integrity
  • Diligent
  • Able to work in a team
  • Demonstrates interpersonal awareness
  • High-energy
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