Quality Control Analyst

Description QC Analyst conducts cGMP testing of final products, in‐process materials, raw materials and stability samples. This person maintains laboratories, assists in writing and optimizing methods, performs method validation and qualification of lab equipment on an as needed basis.

Key Responsibilities:

Perform testing on final products, in‐process materials, raw materials and stability samples Test samples with a variety of methods including chromatography, spectroscopy, wet chemistry and radionuclide assays Complete test records and review data; report any quality anomalies Perform deviation and laboratory investigations, as needed Draft data summaries (i.e. CofA or stability summary table) Write / update SOPs, technical reports, investigations and trend reports Maintain laboratory supplies and chemicals Prepare testing reagents Assist in validation and/or development of analytical methods and techniques Participate in the qualification of QC laboratory equipment Package and send samples to contract laboratories Other duties as assigned Profil souhaité Bachelor's degree in a scientific discipline 0+ years experience in Pharmaceuticals or related industry