What are the responsibilities and job description for the QC Analyst position at Global Life Science Hub?
QC Analyst
Piscataway, NJ - Full-Time
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.