Quality Assurance Lead, Plasma Center

CSL Vifor; Chicago (IL); On-site; USD 36,000 - 40,000; Full time

Job summary

CSL Vifor in Chicago, IL, is seeking a QA-focused role to assist the Assistant Manager of Quality by monitoring plasma center processes and ensuring compliance with SOPs, cGMP, and regulatory requirements. You will report to the AMQ and participate in audits, training, and data reporting for continuous improvement.

The role emphasizes final QA review for shipments, training material maintenance, and collaboration with center management to address deficiencies and corrective actions, while

Qualifications

• Minimum 1-year leadership experience or equivalent of one-year experience in a regulated environment.
• Strong customer service skills.
• Strong critical reasoning, decision-making and problem solving skills to analyze situations.
• Organizational skills and attention to details to handle multiple tasks, short deadlines, frequent interruptions, and shifting priorities in support of changing company objectives.
• Understand Quality Systems and/or regulated training requirements.

Responsibilities

• Perform final QA review and release for all shipment and associated documents, to ensure shipment meets customer specifications.
• Ensure center records QA review to ensure thoroughness, accuracy and timeliness of required information.
• Maintain and review Plasma center personnel training documents to ensure compliance with CSL procedures and regulatory requirements.
• Maintain the Learning Management System to ensure data integrity and reporting.
• Initiate, schedule, coordinate and monitor delivery of all training to meet regulatory requirements.

Skills

Leadership

Customer service

Critical reasoning

Problem solving

Organizational skills

Education

High school diploma or equivalent

Associate or Bachelor’s degree in business administration or biological sciences preferred

Job description

CSL Vifor in Chicago, IL, is seeking a QA-focused role to assist the Assistant Manager of Quality by monitoring plasma center processes and ensuring compliance with SOPs, cGMP, and regulatory requirements. You will report to the AMQ and participate in audits, training, and data reporting for continuous improvement.

The role emphasizes final QA review for shipments, training material maintenance, and collaboration with center management to address deficiencies and corrective actions, while