QC Analyst – Cell and Gene Therapy

Biopatrika; Haryana; On-site; INR 600,000 - 900,000; Full time

Job summary

East Ocyon Bio is hiring a QC Analyst to join the Cell and Gene Therapy quality control team in Gurugram, India. The role involves testing cell therapy products, viral vectors, raw materials and process samples against approved SOPs and specifications, with attention to accuracy and regulatory compliance.

You will perform cell-based assays such as flow cytometry and qPCR/RT-qPCR, operate QC instruments, maintain data with GDP, and support investigations, method qualification and release testing

Qualifications

• 2–3 years of hands‑on experience in a QC lab in biotech, biopharma, cell or gene therapy, or another regulated environment
• Practical experience in at least one of: cell culture-based assays, flow cytometry, qPCR/RT-qPCR or ELISA (more than one is a plus)
• Good working knowledge of GMP, GDP and data integrity
• M.Sc. / M.Tech / B.Tech / B.Sc. in Biotechnology, Microbiology, Life Sciences, Biochemistry or a related field

Responsibilities

• Test cell therapy products, viral vectors, raw materials and process samples against approved SOPs and specifications
• Run cell-based assays, flow cytometry, qPCR/RT-qPCR and/or ELISA
• Operate and maintain QC instruments, and acquire and analyse data
• Keep accurate, traceable records in line with GDP
• Support OOS/OOT and deviation investigations, method qualification and release testing
• Work with Manufacturing, QA and R&D to keep batches moving on time

Skills

QC lab exp

GMP/GDP knowledge

Data integrity

Life sciences background

Education

Biotech/Life Sciences

Job description

We’re Hiring: QC Analyst – Cell and Gene Therapy No. of Positions- 03 East Ocyon Bio is developing off-the-shelf CAR-NK cell therapies for cancer, and our Quality Control team is growing. We’re looking for three QC Analysts with hands‑on lab experience who are careful about documentation.

What you’ll do:

• Test cell therapy products, viral vectors, raw materials and process samples against approved SOPs and specifications
• Run cell-based assays, flow cytometry, qPCR/RT-qPCR and/or ELISA
• Operate and maintain QC instruments, and acquire and analyse data
• Keep accurate, traceable records in line with GDP
• Support OOS/OOT and deviation investigations, method qualification and release testing
• Work with Manufacturing, QA and R&D to keep batches moving on time

What we’re looking for:

• 2–3 years of hands‑on experience in a QC lab in biotech, biopharma, cell or gene therapy, or another regulated environment
• Practical experience in at least one of: cell culture-based assays, flow cytometry, qPCR/RT-qPCR or ELISA (more than one is a plus)
• Good working knowledge of GMP, GDP and data integrity
• M.Sc. / M.Tech / B.Tech / B.Sc. in Biotechnology, Microbiology, Life Sciences, Biochemistry or a related field

Bonus: Skillset focused to CGT, CAR-T or CAR-NK QC testing; viability, purity or potency assays; LIMS Operations; ALCOA+ understanding and compliance.

Location: Gurugram, India