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.

📌 Associate Qc Analyst Charlottetown
🏢 Next Level Group
📍 Charlottetown