About this opportunity
Kedrion Biopharma GmbH lists this Senior QA Specialist: GMP & Compliance Lead opportunity in town of amherst, New York. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Kedrion Biopharma Inc. is seeking a Sr. Quality Assurance Specialist to uphold FDA, EU GMP, and cGMP standards for plasma products. You will review documentation, investigate deviations, and support training and audits to ensure product quality and regulatory readiness.
You will collaborate with Laboratory Management to monitor compliance, improve protocols, and promote continuous improvement across the center’s operations with a focus on data integrity and quality control.
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Who can apply
Review the original listing for work authorization, qualifications and employer requirements.