Quality Associate-i, Qa Assurance-midnight Shift (sunday To Thursday 23:00h-7:30h)

BAXTER HEALTHCARE PTY AUS

Alliston, Ontario, Canada
Base: $72,080 - $108,120 annually; bonus/equity: e...
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Midnight shift sunday to thursday
Gmp regulatory compliance knowledge
Trackwise system experience
** Baxter Healthcare is seeking a Quality Associate to work the midnight shift (Sunday to Thursday) in Alliston, Ontario. The role focuses on maintaining quality and compliance in manufacturing operations, requiring a background in quality assurance within a GMP environment. **

Job Summary

  • The role ensures product and manufacturing operations conform to specifications, Standard Operating Procedures, and Regulatory Standards including Health Canada and FDA.
  • Candidates will support the release process by performing final product releases and managing non-conformance events within the Trackwise system.
  • Baxter is committed to a culture of courage, trust, and collaboration where every individual is empowered to take ownership and make a meaningful impact.

Matching Summary

Match Score: 75

** Baxter Healthcare is seeking a Quality Associate to work the midnight shift (Sunday to Thursday) in Alliston, Ontario. The role focuses on maintaining quality and compliance in manufacturing operations, requiring a background in quality assurance within a GMP environment. **

Salary

Base: $72,080 - $108,120 annually; Bonus/Equity: Estimated target payout under Management Incentive Compensation Plan; Benefits: Not specified

Skills & Requirements

Must-have

  • Midnight shift Sunday to Thursday
  • GMP regulatory compliance knowledge
  • Trackwise system experience
  • Bachelor of Science degree required
  • 3 years manufacturing quality experience

Nice-to-have

  • Lean Six Sigma continuous improvement
  • DMAIC investigation methodology
  • Strong negotiation and communication skills
  • ASQ or other Quality Certification
  • Experience with SPC Infinity systems

Key Requirements

  • Bachelor of Science in Microbiology, Chemistry, Biological Sciences, or Engineering
  • Minimum 3 years of experience in Manufacturing and Quality
  • Previous experience in a GMP environment
  • Intermediate to Advanced proficiency in MS Office Suite

Work Rights

Not specified

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