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 team-oriented 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 Positive 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