Senior Viral Vector Analytics Lead

Tunnell Consulting; Cambridge (MA); On-site; USD 103,000 - 152,000; Full time

Job summary

Tunnell Consulting, an employee-owned life sciences management firm, seeks a Viral Vector Analytics Group Lead for a 3‑month onsite contract in the greater Boston area. You will lead analytical testing strategies for viral vectors, oversee assay development, and ensure regulatory‑compliant QC readiness, working with internal and external partners.

The role requires advanced biology credentials and 8–15 years in viral vector analytics, with strong skills in ddPCR/qPCR, infectious titer, and

Qualifications

• Advanced degree (MS or PhD) in Biology or related field.
• 8–15 years in biopharmaceuticals with viral vector analytics experience.
• Extensive experience with analytical method qualification and validation.
• Strong expertise in one or more viral vector platforms (AAV, lentiviral, adenoviral).
• Hands‑on experience with infectious titer, ddPCR/qPCR, capsid, transgene expression, and potency assays.
• Proven track record as QC lead and in transferring methods to external labs.

Responsibilities

• Serve as technical SME for viral vector analytical methods across development, transfer, and validation.
• Provide scientific leadership for analytical strategies across AAV, lentiviral, and other platforms.
• Lead method qualification/validation and data interpretation for regulatory readiness.
• Coordinate cross‑functional teams to deliver analytical readiness for programs.

Skills

Biology expertise

Viral vector analytics

Analytical leadership

QC leadership

Regulatory knowledge

Education

MS in Biology

PhD preferred

Tools

ddPCR

qPCR

Infectious titer assays

Capsid titer assays

Transgene expression assays

Potency assays

Job description

Tunnell Consulting, an employee-owned life sciences management firm, seeks a Viral Vector Analytics Group Lead for a 3‑month onsite contract in the greater Boston area. You will lead analytical testing strategies for viral vectors, oversee assay development, and ensure regulatory‑compliant QC readiness, working with internal and external partners.

The role requires advanced biology credentials and 8–15 years in viral vector analytics, with strong skills in ddPCR/qPCR, infectious titer, and