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