Senior QC Analyst: HPLC, PCR & Gene Therapy Focus

Kriya Therapeutics, Inc.; Morrisville (NC); On-site; USD 80,000 - 110,000; Full time

Benefits offered by this job

Flexible Time Off

Medical, Dental, and Vision Insurance

Equity

401(k) with Company Match

Parental & Medical Leave

Job summary

Kriya Therapeutics, Inc. seeks an Analyst II or Senior Analyst for Quality Control to perform cGMP testing on production materials, intermediates, and final products. You will author SOPs and QC reports, and mentor laboratory staff as needed.

Responsibilities include leading QC methods across HPLC, CE, PCR and cell-based potency assays, reviewing data, supporting equipment maintenance, and participating in GMP validation activities. Strong documentation and communication are essential.

Qualifications

• BS/BA in Chemistry, Biochemistry, biology or related field.
• 3+ years in cGMP, QC, or similar lab environment.
• Experience with HPLC, PCR, or cell-based potency testing.
• Gene therapy experience is preferred.
• Strong documentation and technical writing skills.
• Excellent verbal and written communication

Responsibilities

• Perform routine and non-routine cGMP testing for samples.
• Provide training support and mentor lab personnel as needed.
• Develop and execute QC methods across multiple techniques.
• Verify and review QC data for accuracy and compliance.
• Lead deviations, CAPAs, and continuous improvement initiatives.
• Serve as SME for assays, instruments, and equipment.
• Support equipment maintenance, calibration, and sample handling.
• Participate in GMP validation activities for lab equipment

Skills

cGMP experience

Documentation practices

Technical writing

Mentoring

Self-directed

Communication skills

Education

Bachelor's degree in Chemistry, Biochemistry, Biological Sciences, or related field

Tools

HPLC

CE

PCR

Cell-based potency assays

Job description

Kriya Therapeutics, Inc. seeks an Analyst II or Senior Analyst for Quality Control to perform cGMP testing on production materials, intermediates, and final products. You will author SOPs and QC reports, and mentor laboratory staff as needed.

Responsibilities include leading QC methods across HPLC, CE, PCR and cell-based potency assays, reviewing data, supporting equipment maintenance, and participating in GMP validation activities. Strong documentation and communication are essential.