Plasma Center Quality Systems Leader

Grifols; Hattiesburg (MS); On-site; USD 85,000 - 115,000; Full time

Benefits offered by this job

Medical benefits

401K plan

Tuition reimbursement

Job summary

Grifols in the United States seeks a Quality Systems Manager to lead quality system processes at the plasma donor center, ensuring SOPs, regulatory compliance, and continuous quality improvement.

You will oversee audits, training programs, CAPA activities, and collaboration with the Center Manager to maintain product quality, donor safety, and staff competency. Strong knowledge of cGMP and FDA regulations is essential.

Qualifications

• Bachelor of Science degree or equivalent.
• Equivalency: Depending on the area of assignment, directly related experience or a combination of directly related education and experience and/or competencies may be considered in place of the stated requirements.
• Typically requires 2 years of related experience in a medical and/or cGMP regulated environment. Experience with plasma or whole blood preferred.

Responsibilities

• Evaluate processes and coordinate strategic quality system improvements at the plasma donor center.
• Maintain the center's quality management system and drive continuous quality improvement.
• Ensure compliance with applicable regulations and implement SOPs for quality control and regulatory compliance.
• Oversee staff training, competency, and training records.
• Collaborate with Center Manager to maintain product quality, donor suitability, and donor safety.

Skills

Interpersonal communication

Problem solving

FDA regulations

Quality management system

Root cause analysis

Documentation skills

Education

Bachelor of Science degree or equivalent

Job description

Grifols in the United States seeks a Quality Systems Manager to lead quality system processes at the plasma donor center, ensuring SOPs, regulatory compliance, and continuous quality improvement.

You will oversee audits, training programs, CAPA activities, and collaboration with the Center Manager to maintain product quality, donor safety, and staff competency. Strong knowledge of cGMP and FDA regulations is essential.