Cell & Gene Therapy QC Validation Lead

Scorpion Therapeutics

Waltham (MA)

On-site

USD 120,000 - 180,000

Full time

8 days ago
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Job summary

Scorpion Therapeutics is seeking a Senior Specialist II, QC Validation, to oversee method validation and validation readiness within Quality Control for cell and gene therapy manufacturing. The role focuses on developing validation strategies, executing activities, and ensuring regulatory compliance across QC operations.

The ideal candidate will have 8+ years (BS) or 6+ years (MS) in GMP QC, with expertise in gene and cell therapy assays, and strong data analysis and quality system knowledge.

Qualifications

  • BS or MS with GMP QC experience (8+ years with BS, 6+ years with MS)
  • Experience with gene and cell therapy assays (qPCR, ddPCR, flow cytometry, ELISA, cell-based assays)
  • Strong GMP, SOP, and quality system knowledge
  • Data analysis skills
  • Experience with method validation for commercial products

Responsibilities

  • Develop validation strategies, protocols, and plans aligned with regulatory standards.
  • Execute validation activities and document results.
  • Analyze data and prepare technical reports.
  • Ensure compliance with GMP and regulatory requirements.
  • Collaborate with Analytical Development, QC testing, QA, and customer teams.
  • Support inspections and audits; mentor supporting staff.

Skills

qPCR
ddPCR
Flow cytometry
ELISA
Cell-based assays
Data analysis
GMP knowledge
SOP knowledge
Quality systems

Education

BS in Biology / Molecular Biology / Chemistry or related field
MS in Biology / Molecular Biology / Chemistry or related field

Tools

LIMS
QMS

Job description

Scorpion Therapeutics is seeking a Senior Specialist II, QC Validation, to oversee method validation and validation readiness within Quality Control for cell and gene therapy manufacturing. The role focuses on developing validation strategies, executing activities, and ensuring regulatory compliance across QC operations.

The ideal candidate will have 8+ years (BS) or 6+ years (MS) in GMP QC, with expertise in gene and cell therapy assays, and strong data analysis and quality system knowledge.

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