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14 August 2026

Quality Associate-II

Ontario, Canada Posted 10 July 2026 Closes 10 September 2026
Department Health & Biotech
Category Health & Biotech
Job type Full-Time
Experience 1 Year

Description

  • Provide front line day-to-day assistance on product quality issues to ensure GMP, regulatory and procedural compliance to maintain high standards of quality.
  • Support during assigned Shift, with the requirement to support plant overtime and planned shutdowns when applicable.
  • Provide technical assistance on review and approval of department-related procedural changes, product quality concerns, reinspections, new product introductions, and protocols.
  • Support timely follow-up on quality exceptions and their preventative/corrective actions.
  • Support initiation/investigation and approvals of non-conformance events in the Trackwise system.
  • Act as SME for Electronic Batch Record (EBR) and SPC or equivalent experience.
  • Perform change control assessments/executions and approvals.
  • Ensure control of defective WIP materials (quarantine, retention, and disposal areas) to keep segregation, movement, documentation, and timely follow-up within the plant in sync with regulatory and compliance requirements.

Qualifications

Highest qualification: University

  • University Degree or equivalent experience, Bachelor of Science or equivalent experience.
  • 1 – 3 years’ experience in manufacturing and quality roles.
  • Prior experience working in a GMP setting.
  • Knowledge of cGMP, ISO, and regulatory standards.
  • Diligent with the ability to work effectively under pressure.
  • Strong written and verbal communication abilities, negotiation capabilities, and the capacity to collaborate with individuals at every level of the organization.
  • Ability to build positive relationships and partner with internal and external collaborators.
  • Strong ability to balance multiple priorities.
  • Strong analytical and problem-solving skills with critical thinking abilities.
  • Intermediate to Advanced proficiency in MS Office Suite.

Preferred Skills

  • 3+ years with exposure to various areas of the manufacturing environment.
  • Experience in pharmaceutical, healthcare, or food manufacturing environments.
  • Experience with continuous improvement methodologies, Lean 6S, Kaizen, TPM, DMAIC.
Quality Associate-II
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