Quality Control Analyst

Global Life Science Hub is partnered with a science-led biologics biotech as they launch a brand-new, state-of-the-art manufacturing facility in New Jersey. Alongside the commercial manufacturing team, the QC organization is being built from the ground up, and we’re hiring 5 QC Analysts at varying seniority levels to establish the laboratory that will underpin all commercial release testing.

With four cutting-edge manufacturing suites and planned scale-up to 6,000L capacity in the next 24–36 months, this site will serve as the engine room for biologics production with QC at the center of ensuring product quality, compliance, and patient safety.

As a QC Analyst, you’ll perform and review cGMP compliant testing to support raw materials, in-process samples, release, and stability programs. You’ll also have the rare opportunity to shape new QC labs, support the site’s first GMP commercial batches, and help implement the latest technologies in biologics testing.

Key Responsibilities

• Execute analytical methods HPLC, SDS-PAGE, ELISA, capillary electrophoresis, cell-based assays, compendial methods for clinical and commercial products.
• Review and document test results, ensuring alignment with cGMP and ICH standards.
• Participate in investigations, OOS, deviations, CAPA, including root cause analysis and closure.
• Collaborate with cross-functional teams, Manufacturing, MSAT, QA to support tech transfer and scale-up activities.
• Support internal/external audits and regulatory inspections.
• Contribute to continuous improvement of QC workflows, instrumentation, and documentation.

Qualifications

• Bachelor’s degree in biotechnology, biochemistry, chemistry, or related field.
• 2–8 years’ experience in a cGMP QC laboratory
• Strong demonstrated hands-on experience in protein chemistry techniques (HPLC, SDS-PAGE, ELISA, capillary electrophoresis, cell-based assays).
• Previous experience authoring/revising SOPs, methods, or technical reports.