Senior QC Specialist – CGT & Flow Cytometry

Germer International

Willow Grove (PA)

Vor Ort

USD 85.000 - 120.000

Vollzeit

Vor 11 Tagen

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Zusammenfassung

Germer International is seeking a QC Specialist II to perform hands-on quality control testing supporting CGT and related products. The role requires expertise in cell-based immunology assays, potency assays, and flow cytometry within a GMP environment.

You will execute routine and non-routine testing, maintain documentation, and collaborate with Manufacturing, QA, Analytical Development, and other QC teams to ensure timely, compliant results.

Qualifikationen

  • Bachelor’s degree in biology, cell biology, immunology, biotechnology, biochemistry, molecular biology, biomedical sciences, or related life science discipline.

Aufgaben

  • Perform routine and non-routine QC testing to support CGT and viral vector manufacturing operations.
  • Execute cell-based immunology assays, potency assays, and flow cytometry.
  • Operate, maintain, and troubleshoot laboratory instruments used for cell-based assays, potency testing, and flow cytometry.
  • Analyze and interpret analytical data to determine if results meet acceptance criteria.
  • Maintain laboratory readiness, equipment status, reagent inventory, and appropriate controls.

Kenntnisse

Flow cytometry
Cell-based assays
Data analysis
Documentation
GMP knowledge
Troubleshooting
Communication
Independent work

Ausbildung

Bachelor’s degree in biology or related life sciences

Tools

LIMS
Veeva Vault QMS
FlowJo
'FACSDiva'
CytExpert

Jobbeschreibung

Germer International is seeking a QC Specialist II to perform hands-on quality control testing supporting CGT and related products. The role requires expertise in cell-based immunology assays, potency assays, and flow cytometry within a GMP environment.

You will execute routine and non-routine testing, maintain documentation, and collaborate with Manufacturing, QA, Analytical Development, and other QC teams to ensure timely, compliant results.

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