Assistant Manager

Scorpion Therapeutics; Hammond (LA); On-site; USD 60,000 - 75,000; Full time

Job summary

Scorpion Therapeutics is seeking an Assistant Manager for a plasma donation center in Hammond, LA. The role oversees donor activities, adherence to regulatory standards, staffing, and overall center efficiency.

Key responsibilities include supervising staff, ensuring FDA compliance, and coordinating with the Center Director. The position emphasizes high-quality donor experiences and rigorous adherence to biopharma quality controls within a hands-on in-center setting.

Qualifications

• 4+ years in the medical field with 2+ years supervisory experience.
• Degree preferred in business or biological sciences; equivalent experience considered.
• Strong knowledge of regulatory requirements and quality standards.

Responsibilities

• Monitor donor flow and center operations to maximize efficiency.
• Oversee staff performance, training, and scheduling.
• Ensure FDA/regulatory compliance and quality control.
• Maintain donor satisfaction and high service standards.
• Coordinate with Center Director and participate in audits and corrective actions.
• Manage supplies and expenses within budget.

Skills

Supervisory experience

Regulatory adherence

Staff performance

Process improvement

Education

Bachelor's degree in business or biological sciences

Job description

Role:

Assistant Manager at a plasma donation center, overseeing donor activities, compliance, staffing, and operational efficiency.

Responsibilities:

monitor donor flow, manage supplies and expenses, ensure regulatory adherence, oversee staff performance and training, and maintain donor satisfaction.

Act as liaison between daily operations and the Center Director, participating in audits and corrective actions.

Requirements:

4+ years in the medical field with 2+ years supervisory experience; college degree in business or biological sciences preferred or equivalent experience.

High-Value:

experience in blood/plasma center operations, FDA and cGMP compliance, staff management, and process improvement.

Work Setup:

based in Hammond, LA; role involves 85% in-center activity, with a focus on high regulatory and quality standards in the biopharma manufacturing context.