Center Manager: Lead Life-Saving Plasma Operations

KEDPLASMA LLC; Florida; On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Health & Wellness

Financial Security

Work-Life Balance

Career Growth

Extra Perks

Job summary

KEDPLASMA, part of Kedrion Biopharma Inc., seeking a Center Manager to lead a plasma donation center and ensure safe, compliant, and efficient operations.

You will drive donor experience, staff performance, and financial results, while maintaining FDA/CLIA/cGMP standards and coordinating with regulatory, quality, and support teams worldwide.

Join a mission-driven team advancing life-saving therapies and building a culture of safety and excellence.

Qualifications

• Minimum 3 years’ management experience in a regulated environment.
• Knowledge of plasma operations and regulatory requirements (FDA, CLIA, cGMP) preferred.
• Experience with P&L and operational performance metrics.
• Strong leadership, communication, and organizational skills.

Responsibilities

• Oversee daily center operations, including quality, compliance, staffing, donor experience, and financial performance.
• Achieve targets for collection volumes, cost efficiency, inventory, donor retention, and profitability.
• Manage recruitment, onboarding, training, and performance evaluations for center staff.
• Ensure timely regulatory documentation and reporting; maintain safety and cleanliness standards.
• Lead staff development, set schedules, and optimize donor wait times.
• Oversee budgeting, payroll, donor fees, and cost control.

Skills

Leadership

Communication

Organizational skills

Regulatory awareness

Travel readiness

Education

Bachelor’s degree in Healthcare/ Life Sciences/ Business Administration

Tools

Microsoft Office Suite

Job description

KEDPLASMA, part of Kedrion Biopharma Inc., seeking a Center Manager to lead a plasma donation center and ensure safe, compliant, and efficient operations.

You will drive donor experience, staff performance, and financial results, while maintaining FDA/CLIA/cGMP standards and coordinating with regulatory, quality, and support teams worldwide.

Join a mission-driven team advancing life-saving therapies and building a culture of safety and excellence.