Lead quality systems for Grifols’ plasma supply chain, applying CAPA management and risk management across regulated donor center operations.
As Quality System Management Manager, you will evaluate processes, develop action plans, and coordinate strategic quality initiatives. You will supervise Quality Assurance and Document and Quality Support Specialists. The position monitors activities affecting product quality, donor suitability, donor safety, and GxP processes while supporting regulatory compliance.
Key Responsibilities:
- Direct documentation, deviation, and CAPA management processes
- Implement robust risk management across supply chain areas
- Establish and evaluate quality system KPIs
- Oversee internal and external audit activities
- Investigate deviations and perform root-cause analysis
Requirements:
- Bachelor’s degree in chemistry, biology, medical technology, or Pharmacy
- At least six years’ Quality Assurance experience
- At least two years in a managerial role
- Experience in cGMP-regulated environments
- Project or technical leadership experience
Apply quality systems, CAPA, risk management, and analytical expertise to support Grifols plasma operations and donor safety.