GMP Scientist II: AAV Vector Production Lead

Valid8 Financial, Inc.; Columbus (OH); On-site; USD 90,000 - 120,000; Full time

Job summary

Andelyn Biosciences, located in Columbus, OH, is seeking a Scientist II Production to learn and lead all aspects of adeno-associated viral vector production under cGMP guidelines. The role coordinates production teams, ensures quality, and supports continuous improvement within a regulated biopharma setting.

Responsibilities include managing daily GMP activities, training staff, maintaining documentation, and upholding regulatory compliance while advancing gene therapy manufacturing.

Qualifications

• Bachelor’s, master’s or PhD in life sciences; biology/biotech preferred.
• 3 years relevant experience with a 4-year degree, or no experience with a Master’s.
• Experience in biologics or gene therapy; highly regulated field preferred.

Responsibilities

• Lead and coordinate production of viral vectors used in clinical trials.
• Oversee GMP manufacturing of AAV drug substances and ensure cGMP compliance.
• Train junior staff and provide SOP training and updates.
• Draft and revise SOPs; maintain documentation per ALCOA principles.

Skills

Four-year degree

Master’s degree

PhD

Life sciences background

Biotech experience

Strong communication

Project management

Independent working

Education

Four-year degree

Master’s degree

PhD

Tools

Microsoft Office

Job description

Andelyn Biosciences, located in Columbus, OH, is seeking a Scientist II Production to learn and lead all aspects of adeno-associated viral vector production under cGMP guidelines. The role coordinates production teams, ensures quality, and supports continuous improvement within a regulated biopharma setting.

Responsibilities include managing daily GMP activities, training staff, maintaining documentation, and upholding regulatory compliance while advancing gene therapy manufacturing.