Operations Supervisor

GRIFOLS, S.A.•CO-Colorado Springs, FL

10d•$22 - $31•Onsite

About The Position

Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions. The Operations Supervisor role is responsible for maintaining the ability to perform any/all tasks within the plasma center, fulfilling the role of production employees and supervising donor flow. This role requires learning and maintaining thorough familiarity and compliance with all state and federal regulations, U.S. Food and Drug Administration (FDA)-approved Standard Operating Procedure Manual, Occupational Safety and Health Administration (OSHA), Clinical Laboratory Improvement Amendments (CLIA), Current Good Manufacturing Practice (cGMP) and internal company procedures. The supervisor oversees donor selection, plasma collection and all manufacturing records to maintain the highest production standards. They attend all required training sessions and staff meetings, ensuring accurate and thorough documentation of necessary records. Under guidance, they ensure the facility is maintained in a neat and clean condition and all equipment is kept in good working order, submitting timely and accurate reports. They assist in the control of center donor funds, assist in training new and current employees, and maintain active communication with other service areas. Building rapport with donors is key to ensuring overall customer satisfaction and supporting long-term donation. They report all unsafe situations or conditions and may be trained to repair plasma center equipment. They assist the Center Manager and/or Assistant Manager in any task necessary in pursuit of company objectives.

Requirements

High school diploma or GED.
Certified as a Phlebotomist, Donor Processor, Plasma Processor, and Designated Trainer.
Typically requires 4 years of related experience with performing phlebotomy, donor processing, and plasma processing duties with demonstrated proficiency to handle difficult situations.

Responsibilities

Maintain the ability to perform any/all tasks within the plasma center; fulfill the role of production employees and supervise donor flow.
Learn and maintain thorough familiarity and compliance with all state and federal regulations, U.S. Food and Drug Administration (FDA)-approved Standard Operating Procedure Manual, Occupational Safety and Health Administration (OSHA), Clinical Laboratory Improvement Amendments (CLIA), Current Good Manufacturing Practice (cGMP) and internal company procedures.
Supervise donor selection, plasma collection and all manufacturing records to maintain the highest production standards in accordance with Federal and State regulations, with FDA approved Standard Operating Procedure Manual, OSHA, CLIA and cGMP.
Attend all required training sessions, staff meetings, etc.
Ensures that accurate and thorough documentation of necessary records is performed.
Under the guidance of the Center Manager and/or the Assistant Manager, assure facility is maintained in a neat and clean condition and all equipment is kept in good working order.
Submit timely and accurate reports as required by the Center Manager and/or the Assistant Manager.
Assist in the control of center donor funds as determined by the Center Manager and/or the Assistant Manager.
Assist in the training of new employees and retraining of current employees.
Maintains active communication with other service areas to ensure accurate documentation and quality.
Builds rapport with donors to ensure overall customer satisfaction with the center to support long-term donation.
Reports all unsafe situations or conditions to area lead, supervisor or manager.
May be trained to repair plasma center equipment.
Assist the Center Manager and/or Assistant Manager in any task necessary in pursuit of company objectives.