Grifols

Operations

• Oversee daily activities of donor floor operations
• Supervise staff and support compliance with regulatory and quality standards
• Ensure execution of operational priorities and provide direct support to the Center Manager
• Create employee schedules to accommodate donor cycles
• Monitor donor flow and address delays or service issues
• Maintain familiar compliance with FDA-approved SOPs and other regulations

Operations Supervisor

• Overseeing the daily activities of donor floor operations
• Supervising staff and supporting compliance with regulatory and quality standards
• Ensures execution of operational priorities and provides direct support to the Center Manager

Manager

• Maintains oversight of the center’s quality management system and ensures continuous quality improvement
• Directs and monitors processes and ensures center compliance with all applicable state, federal, and company-designated regulations
• Implements Standard Operating Procedures (SOPs) for quality control and overall regulatory compliance
• Collaborates with Center Manager to ensure the donor center operates in a manner which assures product quality, donor suitability and donor safety are maintained
• Responsible for the personnel functions of the Quality Systems Associate
• Responsible for oversight of all aspects of internal and external audits
• Continuously assesses, promotes, and improves the effectiveness of the quality and training systems
• Documents, investigates, and performs root-cause analysis for deviations and customer complaints
• Investigates identified trends and performs follow-up on corrective and preventive actions
• Oversees product and biohazard waste shipments
• Performs a review of the documentation of unsuitable test results and unit lookback information
• Ensures that job and center annual training is completed, documented, and on file
• Performs employee training observations to ensure staff competency
• Ensures that all supplies and materials ordered meet quality requirements prior to use and are always stored in appropriate temperature/facility conditions
• Initiates rejection of supplies for non-compliance
• Determines donor suitability activities and manages donor deferrals as appropriate
• Prepares quality analysis reports to track issues and set goals

Quality Manager – Plasma Center

• 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.
• Ensure accurate and thorough documentation of necessary records.
• Ensure 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.
• 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.
• 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.

• 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.

Director

• Support the development of scientifically-sound medical plans in Pulmonology and Critical Care related therapeutic areas.
• Develop and lead Medical Affairs initiatives and strategies aligned with the global and US medical plan to support innovation and company goals.
• Provide medical guidance and consultation to internal stakeholders and educate external customers in therapeutic areas of interest and in support of Grifols existing products and innovation portfolio.
• Build and/or maintain relationships with key opinion leaders and gather insights to inform company strategy and innovation portfolio.
• Serve as the therapy area expert for internal and external stakeholders.
• Provides expert clinical and scientific support to internal teams in the Scientific Innovation Office and commercial functions.
• Support development of global and US medical affairs plans in alignment with business objectives.
• Contribute to commercial strategic planning globally and in the US.
• Build/maintain relationships with scientific thought leaders in Pulmonology and Critical Care and related indications.
• Provide product and disease-specific education and training to internal stakeholders and external customers.
• Participate in and/or facilitate advisory boards, speaker training meetings, symposia, webinars, standalone meetings, etc.
• Review promotional materials and medical information letters to ensure medical accuracy.
• Contribute to the development and execution of publication plans and strategies.
• Review investigator initiated research concepts and proposals and make funding recommendations.
• Serve as a company ambassador during engagements with external patient advocacy organizations.
• Provides strategic input for business development plans and provide scientific/medical review for BD opportunities.
• Attends global and national medical conferences and report key findings and insights to internal stakeholders.
• Partner with patient advocacy, regulatory, HEOR, and market access to support US and global needs.

Senior Medical Affairs Scientific Director

• Acts as the general manager for a Plasma Collection Center and has overall responsibility for the center's operation.
• Manages the daily operations of the center, supervising operations and quality control, and ensuring compliance with all applicable policies and regulations.
• Responsible for meeting quarterly goals, staffing/hours per labor efficiency standards/cost per liter (CPL) targets and Quality key performance indicators (KPI) goals.
• Operates the center and manages employees and operations to the highest standard of ethics and integrity.
• Directs and manages employees. Monitor and evaluate operations. Develop action plans to maximize center efficiency and supervise the implementation of process improvements.
• Manages headcount to provide for efficient staffing through high and low production intervals, providing accurate and timely projections to regional management team in advance of cyclical and seasonal or situational spikes.
• Accountable for donor selection, plasma collection and all manufacturing records to maintain the highest production standards in accordance with state and federal regulations, U.S. Food and Drug Administration (FDA)-approved Standard Operating Procedures, Occupational Safety and Health Administration (OSHA), Clinical Laboratory Improvement Amendments (CLIA), and Current Good Manufacturing Practice (cGMP).

Plasma Center Manager

QA Automation Engineer

• Project Support - Work within a project team, teamwork, schedule adherence, execution, start-up, commissioning, owner interaction, qualifications.
• Provide support in designated area/field such as DCS, PLC, SCADA, BAS, Robotics, Validation.
• Communication - Providing excellent communications (verbal/written) within area of responsibility and demonstrating problem-solving skills.
• Capable of adhering to Good Manufacturing Practices (GxP).
• After hours support may be required.

Automation Engineer II, Senior Automation Engineer I/II, Principal Automation Engineer

Data Scientist

• Serve as a primary insights partner to Commercial leadership.
• Proactively identify business challenges and translate them into analytics-driven solutions.
• Lead analytics for portfolio optimization, therapeutic area (TA) strategy, and in-line brand performance.
• Provide insights to shape strategy.
• Personally develop and oversee the creation of sophisticated scenario models, competitive assessments, and demand forecasts.
• Design and implement advanced models for commercial effectiveness to measure ROI and optimize resource allocation.
• Act as the primary "storyteller," translating complex analyses from disparate data sources into a clear, compelling, and actionable narrative for senior leadership.
• Be a hands-on, collaborative leader, working with data teams to integrate fragmented data sources into a holistic view of the business.

Associate Director, Data Science, Biopharma

QA Engineer

• Evaluate processes and implement quality improvement plans
• Maintain compliance with regulatory standards
• Oversee training programs and audits
• Collaborate with management for quality assurance

Quality Assurance Manager

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

EMT, LVN (Bilingual Preferred)

Basic or Advanced EMT, Bilingual in Spanish

Bilingual EMT/LPN/RN

Bilingual EMT/LVN

• Quality assurance at the plasma donation center: monitoring and ensuring compliance with quality standards and GMP guidelines within regulatory requirements
• Administrative support in the donation center and center-organizational tasks
• Responsibilities include, among others, operational organization, quality assurance and administrative management including inventory and ordering
• Document management, quality management and office organization
• Responding to inquiries from the Human Resources departments
• Preparing reports and statistics (e.g. Excel)
• Supporting the Head of Production

Operations Supervisor

Operations Supervisor

Quality Manager – Plasma Center

Operations Supervisor

Operations Supervisor

Senior Medical Affairs Scientific Director

Plasma Center Manager

Automation Engineer II, Senior Automation Engineer I/II, Principal Automation Engineer

Associate Director, Data Science, Biopharma

Quality Assurance Manager

EMT, LVN (Bilingual Preferred)

Basic or Advanced EMT, Bilingual in Spanish

Bilingual EMT/LPN/RN

Bilingual EMT/LVN

Administrative Assistant, Quality Assurance