Pharma QC Analyst - HPLC & Stability Testing

A leading talent management firm is seeking candidates for a laboratory role in Summit, New Jersey. The responsibilities include assisting with laboratory analysis for clinical release and routine stability testing, conducting analytical experiments and documenting lab work following compliance protocols. Ideal candidates should possess a BS/MS in Chemistry and have 2-4 years of cGMP/GLP experience, alongside skills in HPLC and teamwork. This position represents an excellent opportunity for career advancement in a dynamic environment. #J-18808-Ljbffr