Impact patient care significantly as a Quality Control Specialist in a dynamic biotech workplace. You'll be at the forefront of developing QC processes for critical reagents and consumables.
Ideal candidates should have a Bachelor’s degree in a technical field alongside 5+ years of experience in a cGMP workplace. This position demands hands-on involvement in QC/QA processes and excellent documentation skills, with a focus on cross-functional collaboration across multiple teams including Manufacturing and Engineering.
Key Responsibilities:
• Perform QC activities and batch record reviews
• Partner with teams to establish quality controls
• Manage investigations for OOS issues and CAPAs




• Enhance and document QC processes and work methods
• Engage with multidisciplinary teams during product development
Requirements:
• Bachelor’s degree in a relevant technical field
• Over 5 years in Quality Assurance roles
• Expertise in QC/QA for reagents or IVD manufacturing
• Solid communication and detailed documentation skills
• Ability to work collaboratively across teams
Elevate the quality processes that directly enhance patient outcomes and product effectiveness.
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📌 Quality Control Specialist In Biotech Oakville
🏢 Proven Recruiting
📍 Oakville