Job Title
The Site Validation Lead at CSL Behring plays a critical role in ensuring the quality and compliance of manufacturing processes, guaranteeing the production of high-quality medicines.
This position involves overseeing validation support and staffing for projects, defining validation strategies, and leading process risk assessments. The successful candidate will also develop staff competencies, oversee major projects, and apply validation procedures to ensure global standards and regulatory guidelines are met.
About the Role
* Oversight of validation support and staffing for projects, including resourcing and contingent resources.
* Development of validation strategies and efforts required for registrations, licenses, and changes.
* Maintenance of validated states for manufacturing processes, including cleaning processes.
* Leadership of process risk assessments using defined risk management tools.
* Staff development and competency building within the team.
* Oversee major projects and manufacturing support.
* Application of validation procedures to ensure compliance with global standards and regulatory guidelines.
About CSL Behring
CSL Behring is a global leader in developing and delivering high-quality medicines that treat people with rare and serious diseases. Our treatments offer promise for people in more than 100 countries living with conditions in various therapeutic areas.