Join AtomVie as a Quality Control Analyst, ensuring compliance with GMP regulations while performing critical testing in a dynamic lab setting. Utilize your expertise in analytical chemistry, microbiology, and documentation.

This role requires a College Diploma or B.Sc. in Chemistry or Biotechnology and 1 to 3 years of relevant experience. Responsibilities include conducting quality control testing on drug products and raw materials, documenting results, and maintaining lab equipment. Additionally, you will assist in investigations and ensure regulatory compliance throughout your work.

Key Responsibilities:
• Conduct quality control testing for drug products
• Document analytical data accurately and comprehensively
• Write technical documents,



including Certificates of Analysis
• Perform calibration and maintenance of lab equipment
• Coordinate testing with external labs as needed

Requirements:
• College Diploma or B.Sc. in Chemistry/Biotechnology
• 1-3 years of experience in analytical techniques
• Proficiency with Empower software for data processing
• Strong communication skills in English
• Ability to lift up to 23 kilograms

Bring your analytical skills and attention to detail to AtomVie as a Quality Control Analyst.
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📌 Quality Control Analyst at AtomVie (Ontario)
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📍 Ontario