Quality Systems Associate — QA & Training Lead

Grifols; Clemson (SC); On-site; USD 42,000 - 62,000; Full time

Job summary

Grifols seeks a Quality Systems Associate in Clemson, SC to support quality assurance, training, and regulatory compliance under the Quality Systems Manager. You will review equipment QC, investigate deviations, and help ensure donor safety and product quality.

Responsibilities include training record maintenance, document reviews, and assisting with center audits, SOP adherence, and regulatory alignment to protect product quality and donor safety.

Qualifications

• High school diploma or GED; state licensures/certifications if applicable.
• Typically requires no previous related experience.
• Solid understanding of FDA regulations and cGMP practices.

Responsibilities

• Completes weekly review of equipment QC and maintenance records.
• Documents, investigates, and performs root‑cause analysis for deviations and customer complaints related to product quality and/or donor safety.
• Inspects and releases incoming supplies; investigates and reports non-compliant supplies.
• Performs documentation review for unsuitable test results.
• Assists QSM to ensure SOPs and regulatory requirements are followed.
• Performs all product release activities.
• Reviews lookback information and donor center documents.

Skills

Interpersonal skills

Organizational skills

Problem solving

FDA regulations

Quality compliance

Mathematics knowledge

Legible handwriting

Computer proficiency

SOP adherence

Education

High school diploma or GED

Job description

Grifols seeks a Quality Systems Associate in Clemson, SC to support quality assurance, training, and regulatory compliance under the Quality Systems Manager. You will review equipment QC, investigate deviations, and help ensure donor safety and product quality.

Responsibilities include training record maintenance, document reviews, and assisting with center audits, SOP adherence, and regulatory alignment to protect product quality and donor safety.