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CQV Associate II — GMP Biopharma Automation & Validation

Job in Hamilton, Ontario, E8H, Canada
Listing for: OmniaBio Inc
Full Time position
Listed on 2026-01-04
Job specializations:
  • Engineering
    Validation Engineer
Job Description & How to Apply Below
A leading biotechnology firm in Hamilton, Ontario is seeking an Associate II for Commissioning, Qualification and Validation. This role involves developing validation plans, collaborating with internal teams, and ensuring compliance with GMP standards. Candidates should have over 3 years of relevant experience in a GMP environment, a postsecondary education in engineering technology, and strong communication skills. Omnia Bio offers a dynamic workplace focused on innovation in cell and gene therapies.
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Position Requirements
10+ Years work experience
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