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)