Quality Assurance Specialist (Laboratory)

Quality Assurance Specialist (Laboratory) Location: Amherst, New York | Employment Type: Contract | Pay Range: $20.10 – $27.00 per hour Job Summary: Are you detail-oriented and passionate about quality and compliance? Join our team as a Quality Assurance Specialist and help ensure the safety and integrity of life‑saving plasma products. In this role, you’ll be a key player in upholding regulatory standards and supporting continuous improvement across the center’s operations. As a Quality Assurance Specialist, you’ll work closely with the Quality Assurance Manager and center leadership to monitor compliance, review documentation, and support training and audit readiness. Your work will directly impact donor safety and product quality. What you’ll do Review manufacturing activities and documentation to ensure compliance with SOPs and regulatory requirements. Identify and escalate non‑compliance issues that could affect donor safety or plasma quality. Support plasma release and shipment processes, ensuring all units meet specifications. Investigate deviations and assist in implementing corrective actions. Audit records for completeness, consistency, and accuracy to maintain data integrity. Monitor equipment qualification, calibration, and maintenance documentation. Ensure proper storage and documentation of supplies, reagents, and equipment. Perform quality control checks on stored and shipped products, as well as test reagents. Track and trend quality data to identify improvement opportunities. Participate in internal audits and support external inspections. Assist in training staff on quality procedures and ensure training records are up to date. Evaluate staff competency through direct observation, written assessments, and proficiency testing. Promote a culture of continuous improvement and regulatory excellence. Qualifications and need‑to‑know Bachelor’s degree in life sciences or a related field preferred. Minimum two years’ experience in a laboratory setting, preferred. Ability to analyze data and identify trends. Strong organizational and documentation skills. Familiarity with FDA, EU GMP, and cGMP standards. Excellent communication and collaboration skills. Comfortable working in a highly regulated environment with exposure to bloodborne pathogens and cold storage areas. Proficiency in Microsoft Office and data entry systems preferred. Employment eligibility verification will be required at the time of hire. This position does not offer visa sponsorship now or in the future. Kedrion Biopharma Inc. is committed to providing equal employment opportunities to all employees and applicants. We prohibit discrimination and harassment based on race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. This policy applies to all employment terms, including recruitment, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training. Salary ranges are determined based on relevant experience, education, and certifications. If you require assistance with your employment application or need reasonable accommodations to perform job duties, please contact our Talent Acquisition team at View email address on click.appcast.io . Employee Benefits: Health & Wellness – Full medical, dental, and vision coverage Financial Security – Life insurance, AD&D, and retirement savings plans Work‑Life Balance – Paid time off, sick leave, and paid holidays Career Growth – Training programs and development opportunities Extra Perks – Employee discounts, wellness initiatives, and more! For specific inquiries please reach out to us. Kedrion Biopharma Inc. participates in E‑Verify and provides the federal government with Form I‑9 information to confirm employment authorization. #J-18808-Ljbffr