- Madison, Wisconsin, United States
- On-site
- 2+ years
Lead a team of validation professionals, maintain validation master plans, review and approve validation protocols and reports, support commissioning, qualification, and validation activities, manage requalification programs, participate in audits and inspections, drive continuous improvement initiatives, serve as validation SME, coordinate with QA, manufacturing, facilities, engineering, and customers, provide technical training and support.
Responsibilities
- Lead a team of Validation professionals.
- Maintain Validation Master Plans.
- Review and approve validation protocols and reports.
- Support commissioning, qualification, and validation activities.
- Review Change Controls.
Requirements
- Doctorate in a STEM field
- Master’s degree in a STEM field
- Bachelor’s degree in a STEM field
- Nice to have: pharmaceutical manufacturing
- Nice to have: biologics manufacturing