Potency Assay Scientist - Gene Therapy (Associate)

Spectraforce Technologies, Inc.; East Hanover (NJ); On-site; USD 65,000 - 90,000; Full time

Job summary

Spectraforce Technologies, Inc. is seeking a Scientific Associate (Associate Expert Potency) in East Hanover, NJ to support development activities for gene therapy analytics. The role involves performing and qualifying cell-based potency assays and contributing to cross-functional processes for continuous improvement.

The candidate will work onsite in a fast-paced team, handling sample testing, data analysis, and regulatory documentation while ensuring compliance with GxP and safety requirements.

Qualifications

• MS in Biology, Biochemistry, Bioengineering or related field with 0–2 years’ research, or BS with 4 years’ equivalent.
• Basic understanding of cell biology and protein chemistry.
• Experience with cell culture and aseptic techniques required.
• Exposure to bioassays and analyzing multiple assay platforms is expected.
• Strong communication and ability to work in a fast-paced team.

Responsibilities

• Participate in method development and qualification of cell-based potency assays for AAV and LVV vectors.
• Support phase-appropriate bioassay development and data analysis for regulatory filings.
• Manage critical reagents, in-process samples, and assay transfers to QC/ CRO labs.
• Document protocols, summaries, and test results with clear records.
• Maintain inventory and support routine lab activities.

Skills

Communication skills

Team collaboration

Detail oriented

Fast-paced work

GxP familiarity

Education

MS in Biology/Biochemistry/Bioengineering

BS with 4 years equivalent

Tools

ELISA

MSD

High-content imaging

qPCR

dPCR

Job description

Spectraforce Technologies, Inc. is seeking a Scientific Associate (Associate Expert Potency) in East Hanover, NJ to support development activities for gene therapy analytics. The role involves performing and qualifying cell-based potency assays and contributing to cross-functional processes for continuous improvement.

The candidate will work onsite in a fast-paced team, handling sample testing, data analysis, and regulatory documentation while ensuring compliance with GxP and safety requirements.