Quality Systems Leader - Donor Center Excellence

Grifols, S.A

Goldsboro (NC)

On-site

USD 90,000 - 130,000

Full time

11 days ago

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Benefits offered by this job

Medical benefits
PTO
401K match
Tuition reimbursement

Job summary

Grifols, S.A seeks a Quality Systems Manager (QSM) to lead the plasma donor center's quality management, training, and regulatory compliance. You will design and implement SOPs, manage audits, and drive corrective actions to ensure product quality and donor safety.

The role requires a BS degree or equivalent and 2+ years in a cGMP-regulated environment, preferably with plasma experience. Location: Goldsboro, NC; travel may be needed.

Qualifications

  • Bachelor of Science degree or equivalent required.
  • 2 years of related medical or cGMP experience.
  • Experience with plasma or whole blood preferred.

Responsibilities

  • Evaluate processes and coordinate strategic implementation of quality system processes.
  • Maintain oversight of the quality management system and drive continuous improvement.
  • Direct compliance with applicable regulations and implement SOPs for quality control.
  • Oversee staff training records and ensure competency.
  • Collaborate with Center Manager to ensure product quality and donor safety.
  • Oversee audits, CAPAs, and corrective/preventive actions.
  • Prepare quality analysis reports and track issues to goals.

Skills

Interpersonal communication
Organizational skills
Problem solving
FDA regulations
Quality & compliance
Mathematics
Computer proficiency
Root cause analysis
Corrective actions
Preventive actions
Time management
Travel readiness
Center leadership

Education

Bachelor of Science degree
BS degree

Job description

Grifols, S.A seeks a Quality Systems Manager (QSM) to lead the plasma donor center's quality management, training, and regulatory compliance. You will design and implement SOPs, manage audits, and drive corrective actions to ensure product quality and donor safety.

The role requires a BS degree or equivalent and 2+ years in a cGMP-regulated environment, preferably with plasma experience. Location: Goldsboro, NC; travel may be needed.

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