Job Description
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
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