In-Process QC Analyst – Biopharma, GMP

A biopharmaceutical company in Tustin, California, seeks a Quality Control In-Process Analyst to perform testing and sampling in a GMP environment. Responsibilities include conducting QC testing, writing procedures, and collaborating with departments on QC protocols. The role requires a BS in a related field and 2 years of biotech experience. Competitive compensation, with a salary range of $26.73 to $35.63 per hour, is offered alongside various benefits. #J-18808-Ljbffr