Grifols

Bilingual

• Perform physical examination and establish medical history to determine donor suitability
• Build rapport with donors to ensure overall customer satisfaction
• Ensure donor and staff confidentiality
• Responsible for donor awareness to potential hazards
• Provide donor education regarding general health and provide counseling regarding unacceptable test results
• Evaluate & manage donor injuries and adverse events
• Perform evaluations of any history of illness or medications to ensure continued donor suitability
• Assist in employee training
• Administer employee Hepatitis Vaccine program

Bilingual LVN, RN – Spanish

Manager

• Serve as GT Manufacturing System Owner for EBR/MES Systems and associated digital systems, aligning with global governance expectations, testing standards, and change management.
• Own the site level configuration, functional administration, SOP’s, and lifecycle management of EBR/MES, and manufacturing IT systems.
• Coordinate and support recipe validation workflows, including SAP‑impacted and non‑SAP‑impacted changes, in alignment with site change management processes.
• Collaborate with site Quality as the GT Manufacturing Digital Systems representative to the Data Integrity Program for digital manufacturing control systems, ensuring alignment with regulatory and global corporate standards.
• Act as the system owner and primary GT Manufacturing lead for the functional management of Maximo, the GT site CMMS system.
• Lead site level functional integration initiatives between EBR, SAP, process automation systems, process historians, and other digital sources (e.g., logbooks, automation HMIs).

Manufacturing Digital Manager

Operations

• Oversees donor operations and supervises Operation Supervisor(s) and donor center staff during assigned shifts
• Maintains the ability to perform any/all tasks within the plasma center
• Creates employee schedules to accommodate donor cycles
• Determines the adequacy and adjusts inventory levels of all goods and supplies necessary for the operation
• Keeps Center Manager informed of any irregularities within the center
• Supports and executes daily operational plans to achieve center performance targets
• Monitors donor flow and proactively addresses delays or service issues
• Learns and maintains thorough familiarity and compliance with all state and federal regulations
• Supervises donor selection, plasma collection and all manufacturing records
• Submits timely and accurate reports as required by the Center Manager
• Participates in the onboarding, training, and cross-training of staff

Senior Operations Supervisor

EMT, Bilingual in Spanish

EMT/EMTB – Bilingual in Spanish

• Support shipping and receiving activities
• Support new employee onboarding activities
• Maintain and clean office appliances
• Unpack and organize incoming packages
• Perform invoice management of received goods
• Serve as point of contact for delivery personnel and lab vendors
• Update and maintain operational databases and systems
• Assist with data documentation (scanning/printing)
• Assist with inventory counts and maintenance of office and lab spaces
• Perform daily stocking of office goods and weekly stocking of laboratory supplies
• Assist with company events with set up and clean up
• Support facility safety by maintaining fire extinguishers, eye wash stations and showers
• Maintain records of equipment documentation
• Support staff in organization activities
• Assist in furniture and equipment moves
• Perform general lab cleaning duties
• Prepare and aliquot lab reagents
• Support laboratory specialty gas systems and supply

Operations Assistant

Engineer

• Demonstrates consistent application of technical knowledge and/or regulatory knowledge in Engineering disciplines
• Executes assignments of medium complexity, developing solutions for defined problems
• Provides engineering project support related to the design and implementation of both new and upgraded facilities, systems and equipment used in manufacturing
• Sustains facilities compliant with the FDA's Good Manufacturing Practice Regulations
• Collaborates with other functional areas in Engineering, Manufacturing, Quality, Regulatory, etc.

Engineer III – Manufacturing and Automation, GMP

• 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
• Attend all required training sessions, staff meetings, etc
• Ensure accurate and thorough documentation of necessary records is performed
• Assure facility is maintained in a neat and clean condition
• 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
• Maintain active communication with other service areas to ensure accurate documentation and quality
• Build rapport with donors to ensure overall customer satisfaction with the center to support long-term donation
• Report all unsafe situations or conditions to area lead, supervisor or manager

Operations Supervisor

• Responsible for all aspects of the donor center when the Center Manager is not present.
• Collaborates with Training and Quality staff to ensure that training and quality goals are met.
• Coaches and leads through effective feedback to employees through the Operations Supervisor(s).
• Monitors and evaluates operations.
• Works with the Center manager to develop action plans to maximize center efficiency and supervises the implementation of improvements.
• Makes critical decisions for the modifications of action plans.

Plasma Center Operations Manager

• Supervise donor selection, plasma collection and all manufacturing records
• Maintain the highest production standards in accordance with Federal and State regulations
• 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
• Report all unsafe situations or conditions to area lead, supervisor or manager

Designer

• Contribute to system design for utilities such as Steam, Chilled Water, Natural Gas, and Plumbing
• Develop construction documents for underground plumbing systems
• Specify utility equipment and perform vendor evaluations
• Lead installation and supervision during construction
• Analyze existing utility systems for improvements

Industrial Mechanical Systems Design

QA Engineer

• Manage product release activities, evaluating technical and documental compliance according to Technical Direction guidelines
• Participate in the configuration of systems related to product release
• Coordinate communications with Notified Bodies, reference laboratories and related stakeholders
• Manage documentation storage, control and retrieval, including externally archived documentation
• Handle document management quality notifications, ensuring proper tracking and workflow
• Approve quality notifications after evaluating their impact on batch release and product status
• Monitor the status of materials affected by quality notifications
• Coordinate communications with Health Authorities (e.g., AEMPS) regarding import/export activities
• Issue and manage authorizations and official letters required for import/export processes
• Ensure compliance with applicable regulations such as ISO 13485, IVDR and MDSAP
• Act as internal auditor and participate in supplier audits
• Participate in continuous improvement of the Quality Management System.

QA Product Release Section Manager

Basic or Advanced EMT, Paramedic, LVN, Bilingual in Spanish Preferred

LVN, Bilingual in Spanish

Data Analyst

• Manage the KPI application and database and generate and distribute monthly reports
• Manage the QUINTET application and database and generate and distribute monthly reports
• Generate compliance metrics based on external inspection and internal audit data
• Work with other departments on periodic updates of existing and potential metric and KPI parameters
• Generate various reports on periodic basis for distribution within Biomat USA and other Grifols entities
• Assist in developing additional mechanisms for assessing data and quality analytics within the organization
• Supports the improvement of analytic development lifecycle as solutions and applications are developed and implemented
• Continuously assess existing systems, applications and databases for improvements. Work with other departments on periodic updates
• Assists in additional quality monitoring initiates (i.e. Risk Assessment, Data Integrity, Corporate Deviation Management), when applicable
• Assists in the development and ongoing updates of cGMP operating procedures that relate to Quality analytics and associated functions.

Bilingual LVN, RN – Spanish

Manufacturing Digital Manager

Senior Operations Supervisor

EMT, Bilingual in Spanish

EMT/EMTB – Bilingual in Spanish

Operations Assistant

Engineer III – Manufacturing and Automation, GMP

Operations Supervisor

Plasma Center Operations Manager

Operations Supervisor

Industrial Mechanical Systems Design

QA Product Release Section Manager

Basic or Advanced EMT, Paramedic, LVN, Bilingual in Spanish Preferred

LVN, Bilingual in Spanish

Quality Analytics Specialist