Job description

Mission
Join our client’s Site Validation team to keep biological drug-substance operations compliant while an internal role is back-filled. After September, continued involvement is likely given the strong project pipeline.

Key Responsibilities

• Execute routine qualification & validation protocols for small-scale equipment


• Adapt process parameters and recipes under GMP


• Perform non-CSV validations: building, drug-substance production equipment, periodic reviews


• Contribute to ad-hoc project work as integration and skills allow

Must-Have