Quality Systems & Training Associate - cGMP | Donor Center

Grifols; Clemson (SC); On-site; USD 42,000 - 64,000; Full time

Job summary

Grifols is hiring a Quality Systems Associate to support quality assurance and training within our donor center operations. Under the supervision of the Quality Systems Manager, you will perform QA tasks to ensure compliance with internal and external regulations and protocols.

Primary responsibilities include reviewing equipment QC, investigating deviations, releasing supplies, and assisting with center training programs to uphold cGMP standards.

Qualifications

• Strong problem-solving and analytical ability.
• Understanding of FDA regulations and quality systems.
• Attention to detail and document control.
• Proficiency with computers and basic math.
• Good handwriting and clear communication.

Responsibilities

• Completes weekly review of equipment QC and maintenance records.
• Documents, investigates, and performs root-cause analysis for deviations and customer complaints.
• Inspects and releases incoming supplies and reviews related documentation.
• Ensures compliance with cGMP, SOPs, and regulatory requirements.
• Performs product release activities and reviews donor center documentation.

Education

High school diploma

Job description

Grifols is hiring a Quality Systems Associate to support quality assurance and training within our donor center operations. Under the supervision of the Quality Systems Manager, you will perform QA tasks to ensure compliance with internal and external regulations and protocols.

Primary responsibilities include reviewing equipment QC, investigating deviations, releasing supplies, and assisting with center training programs to uphold cGMP standards.