Primary responsibilities:

• Perform various scientific analyses to evaluate the quality of raw materials, in-process materials, and finished goods to ensure compliance with established standards, including conducting and validating various biological and chemical quality control (QC) assays.
• Compiling, interpreting, and documenting statistical data obtained from testing process and will verify to confirm compliance with established quality standards or identify any deviations.
• Organizing and ensuring that the appropriate value assignments, proficiency surveys and certification programs are scheduled, performed, and reported.
• May include establishing specifications for conducting assays and writing standard operating procedures.

To succeed in this role:

• Excellent organizing skills, time management skills and communication skills.
• Ability to read, write, and follow technical documentation in English.
• Detailed-oriented and skilled at diagnostics test methods and interpreting results.
• Possess post-secondary education in a related field with a minimum of 2 years of related experience, preferably in a clinical chemistry and quality control.
• Automated clinical chemistry analyzer experience would be an asset.