Quality Assurance Specialist — Impact Safe Plasma

KEDPLASMA LLC; Florida; On-site; USD 55,000 - 85,000; Full time

Benefits offered by this job

Health coverage

Retirement plans

Paid time off

Career growth

Employee discounts

Job summary

Kedrion Biopharma Inc. seeks a Quality Assurance Specialist to uphold regulatory standards and support continuous improvement across the plasma center. You will work with leadership to monitor compliance, review docs, and train staff to maintain donor safety and product quality.

Ideal candidates have a life sciences background, experience in regulated environments, and strong data analysis and collaboration skills. This role is based in Florida with on-site duties and comprehensive benefits.

Qualifications

• Bachelor’s degree in life sciences or related field required.
• Minimum 1 year of experience in a regulated industry preferred.
• Familiarity with FDA, EU GMP and cGMP standards is advantageous.
• Excellent communication and collaboration skills.

Responsibilities

• Review manufacturing activities and documentation for compliance with SOPs and regulations.
• Identify and escalate non-compliance issues affecting donor safety or plasma quality.
• Support plasma release and shipping ensuring units meet specifications.
• Investigate deviations and assist in corrective actions.
• Audit records for completeness and accuracy to maintain data integrity.
• Monitor equipment qualification, calibration, and maintenance docs.
• Ensure proper storage and documentation of supplies, reagents, and equipment.
• Perform quality control checks on products and test reagents.

Skills

Data analysis

Organizational skills

Communication

Collaboration

Attention to detail

Education

Bachelor’s degree in life sciences or related field

Tools

Microsoft Office

Job description

Kedrion Biopharma Inc. seeks a Quality Assurance Specialist to uphold regulatory standards and support continuous improvement across the plasma center. You will work with leadership to monitor compliance, review docs, and train staff to maintain donor safety and product quality.

Ideal candidates have a life sciences background, experience in regulated environments, and strong data analysis and collaboration skills. This role is based in Florida with on-site duties and comprehensive benefits.