QC Analyst

We are placing QC Analysts with a leading biosimilars manufacturer in Piscataway, NJ. You will be performing analytical testing and data verification supporting late-stage clinical and commercial small molecule and biosimilar products in a cGMP laboratory. Strong protein chemistry background required, with hands‑on HPLC testing as a core focus. What you’ll be doing: Analytical testing to support in-process, release, raw materials, and stability programs Performing and troubleshooting HPLC, SDS‑PAGE, cell‑based bioassays, capillary electrophoresis, and ELISA Supporting Out of Specification investigations, deviations, and CAPA plans Authoring and reviewing SOPs, technical documents, and reports Collaborating cross‑functionally to advance projects and resolve lab investigations What you need: 2-3+ years of QC laboratory experience in a cGMP pharmaceutical or biotech environment Background in protein chemistry with HPLC testing experience Comfortable troubleshooting analytical results and writing SOPs Knowledge of Empower and/or Shimadzu software a plus Bachelor’s degree in biotechnology, biochemistry, chemistry, or related field Apply directly or get in touch to discuss. #J-18808-Ljbffr