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 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.