Hiring: Quality Manager Company: Grifols Location: Sumter, SC Job Posted Time: 2026-09-14 14:03:28 Target Skills & Keywords : Regulatory Compliance, Root Cause Analysis About the job Experience: •2 years of related experience in a medical and/or cGMP regulated environment. Experience with plasma or whole blood preferred. •10 years — we’re growing, and you can grow with us! Required Skills: •Evaluates processes, develops action plans, and coordinates the strategic implementation of quality system processes and corrective actions at the plasma donor center. •Maintains oversight of the center’s quality management system and ensures continuous quality improvement, by addressing deficiencies in a timely manner and communicating concerns to the appropriate parties. •Directs and monitors processes and ensures center compliance with all applicable state, federal, and company-designated regulations. Implements Standard Operating Procedures (SOPs) for quality control and overall regulatory compliance. •Maintains oversight of center training program by ensuring compliance to program requirements promoting staff competency in their assigned job duties. Maintains and audits training records and files. •Collaborates with Center Manager to ensure the donor center operates in a manner which assures product quality, donor suitability and donor safety are maintained. •Lead and oversee the personnel functions of the Quality Systems Associate; including direction, assignment of work, hiring, development and training, disciplinary actions, termination, maintenance of personnel records, work schedule and delegation/follow-up of tasks. •Lead and oversee oversight of all aspects of internal and external audits including audit preparation, execution, response, implementation of corrective/preventative actions, assessment of corrective actions, and follow-up as required. •Continuously assesses, promotes, and improves the effectiveness of quality and training systems in the donor center through recognition of trends, investigation of failures in the execution of procedures, and direct observations. Qualifications: •Bachelor of Science degree or equivalent. •Typically requires 2 years of related experience in a medical and/or cGMP regulated environment. Experience with plasma or whole blood preferred. •Works independently with little guidance or reliance on oral or written instructions and plans work schedules to meet goals. •Frequently interacts with others, relates sensitive information to diverse groups. Must work with diverse groups to obtain consensus on issues. •Demonstrated capacity to apply abstract principles to solve complex conceptual issues. •4 years of experience, an equivalency could include 8 years of experience, an associate degree with 6 years of experience, or a master’s degree with 2 years of experience. Compensation: •We offer benefits including medical, PTO, up to 5% 401K match, and tuition reimbursement Interested candidates, please apply directly through the job posting on company's career page or try via AI auto apply on this platform. Don't miss this opportunity to join a forward-thinking team!