OmniaBio: Associate II, Commissioning, Qualification and Validation

CCRM and OmniaBio

4 months ago

Hamilton, ON

Onsite

Full Time

Medior

0 applicants

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About this role

A Associate II, Commissioning, Qualification and Validation, supports validation activities for manufacturing facilities, equipment, and systems in a biopharma environment to ensure compliance with GMP standards. The role involves documentation development, risk assessments, audits, and collaboration with various stakeholders to maintain validation integrity.

Skills

Qualifications

3+ years in CQVPostsecondary education in engineering technology

About CCRM and OmniaBio

omniabio.com

OmniaBio is a contract development and manufacturing organization (CDMO) focused exclusively on cell and gene therapies. The company offers specialized, efficient services to advance programs from preclinical development through commercial‑scale manufacturing. OmniaBio positions itself as a partner that brings maturity to the cell and gene therapy sector by delivering scalable processes, development and manufacturing expertise, and regulatory‑aware solutions to accelerate translation and commercialization.