Our biopharmaceutical client is seeking a highly skilled QC Analyst to support analytical testing and data verification in a GMP-regulated laboratory. This position will play a critical role in ensuring the accuracy and reliability of data that support in-process, release, raw materials, and stability programs.
Pay rate: $30/ hr.- $33/ hr.
Job type: Contract-hire
Location: Middlesex County, NJ
Essential Duties & Responsibilities:
- Conduct analytical testing to support in-process, release, raw materials, and stability programs
- Perform bioassays and chemical analysis using a variety of methods
- Review, analyze, and report analytical data
- Collaborate with internal teams to ensure high-quality outcomes and compliance with regulations
Qualifications:
- Bachelor's degree in Biology, Chemistry, Biochemistry, or a related field
- Minimum of 2 years of relevant QC experience (Biopharma)
- Previous experience in a cGMP-regulated laboratory
- Proficient in analytical techniques including: HPLC (High-Performance Liquid Chromatography), SDS-PAGE (Sodium Dodecyl Sulfate Polyacrylamide Gel Electrophoresis), Cell-based bioassays, ELISA (Enzyme-Linked Immunosorbent Assay)