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Grifols

Quality Manager

Grifols

. Evaluate processes, develop action plans, and coordinate strategic implementation of quality system processes and corrective actions at the plasma donor center .

Posted 10/2/2026full-timeToledo • Ohio • United StatesMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in quality management systems, regulatory compliance, and training oversight within a plasma donor center. Proficient in conducting audits, root-cause analysis, and preparing quality analysis reports to ensure continuous improvement and donor safety.

Highest-signal resume keywords
Quality Management System OversightRegulatory Compliance ImplementationRoot-Cause AnalysisInternal and External AuditsCLIA Proficiency Testing Knowledge

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Standard Operating Procedures (SOPs)Quality ControlQuality Analysis ReportingDeviations InvestigationDonor Suitability ManagementTraining System OversightCorrective/Preventive ActionsTrend RecognitionBiohazard Waste ManagementCustomer Complaint Investigation
Soft Skills
CollaborationLeadershipCommunicationTraining and DevelopmentProblem-Solving
Certifications & Qualifications
Bachelor of Science Degree
Industry Keywords
Plasma Donor CenterQuality ImprovementRegulatory DocumentationState and Federal RegulationsDonor Deferrals

About the role

Key responsibilities & impact
  • Evaluate processes, develop action plans, and coordinate strategic implementation of quality system processes and corrective actions at the plasma donor center
  • Maintain oversight of the center’s quality management system and drive continuous quality improvement
  • Direct and monitor processes for regulatory compliance and implement quality-control SOPs
  • Oversee the center training program, training records, and staff competency
  • Collaborate with the Center Manager to maintain product quality, donor suitability, and donor safety
  • Manage personnel functions for the Quality Associate, including work assignment, hiring, development, training, discipline, termination, scheduling, and task follow-up
  • Oversee internal and external audits, corrective/preventive actions, and follow-up
  • Assess quality and training system effectiveness through trend recognition, failure investigation, and direct observation
  • Document, investigate, and perform root-cause analysis for deviations and customer complaints
  • Investigate trends and assess the effectiveness of corrective/preventive actions and process improvements
  • Oversee product and biohazard waste shipments, labeling, documentation, and final shipment authorization
  • Review unsuitable test results, unit lookback information, donor adverse event reports, and related documentation
  • Ensure annual job and center training is completed and documented
  • Conduct employee training observations before independent work release
  • Verify supplies and materials meet quality requirements and are properly stored; investigate or reject non-conforming supplies
  • Determine donor suitability, manage donor deferrals, and review deferred donor reinstatements
  • Prepare quality analysis reports and research systemic compliance issues
  • Ensure CLIA proficiency test surveys, complaint investigations, and training are documented
  • Hold monthly Quality Meetings to communicate updates and manage action outcomes

Requirements

What you’ll need
  • Bachelor of Science degree or equivalent
  • Knowledge of applicable state, federal, and company-designated regulations
  • Ability to implement Standard Operating Procedures (SOPs) for quality control and regulatory compliance
  • Ability to oversee quality management and training systems
  • Ability to conduct internal and external audits
  • Ability to investigate deviations and customer complaints and perform root-cause analysis
  • Ability to oversee product and biohazard waste shipments and related regulatory documentation
  • Knowledge of Clinical Laboratory Improvement Amendments (CLIA) proficiency testing
  • Ability to manage donor suitability activities and donor deferrals
  • Ability to prepare quality analysis reports and perform in-depth research and analysis

Benefits

Comp & perks
  • Equal employment opportunity protections
  • Regular full-time employment