Apply HPLC, GC, KF, and wet chemistry expertise as a Quality Control Analytical Chemist with Eurofins CDMO Alphora in Ontario. Rotating shifts are required.

This Quality Control Analytical

Chemist I supports cGMP pharmaceutical manufacturing operations for active pharmaceutical ingredients. The role tests raw materials, in-process controls, intermediates, and finished products. You will interpret results, support investigations, and maintain laboratory compliance within a cooperative QC team.

Key Responsibilities: Test raw materials, intermediates, and finished products Perform in-process control testing for cGMP operations Interpret results, tabulate data, and generate reports Identify out-of-specification results and assist investigations Perform equipment calibration checks and performance verifications Requirements: Diploma or degree in a related field Practical HPLC, GC, KF, and wet chemistry experience Understanding of current Good Manufacturing Practices Excellent documentation, communication, and organizational skills Ability to work rotating shifts with minimal supervision Build pharmaceutical quality control experience through analytical testing, cGMP support, and laboratory compliance at Eurofins CDMO Alphora.

📌 Quality Control Analytical Chemist HPLC GC (Oakville)
🏢 Eurofins Group
📍 Oakville