Quality Control Analytical Chemist I - Eurofins CDMO Alphora, Inc.
Core
Perform analytical testing of raw materials, in-process controls, intermediates, and finished products to ensure compliance with cGMP for pharmaceutical API manufacturing.
Role type
Quality Control Analytical Chemist
Builds
Safe and efficacious pharmaceutical Active Pharmaceutical Ingredients (APIs) and finished dosage products
Domain
Pharmaceutical manufacturing / Contract Development and Manufacturing Organization (CDMO)
Required skills
HPLC, GC, KF, wet chemistry techniques, cGMP compliance, OOS investigation, equipment calibration
Preferred skills
GCMS, LCMS, Ion Chromatography, documentation skills, problem-solving
Technologies
HPLC, GC, GC/Headspace, IR, GCMS, LCMS, Ion Chromatography
Responsibilities
Testing raw materials, in-process controls, intermediates, and finished products; Interpret and report test results; Identify and assist in investigating OOS results; Perform calibration checks and performance verifications of laboratory equipment; Work in accordance with cGMP and safety requirements
Seniority
Entry-level to Mid-level, hands-on IC
