Grifols

Nurse

• Build rapport with donors to ensure overall customer satisfaction
• Select suitable plasmapheresis donors by performing physical examinations and taking medical histories
• Follow the FDA-approved Standard Operating Procedure Manual, current state and federal guidelines, OSHA, CLIA, CGMP, internal company procedures, education, and experience
• Ensure donor and staff confidentiality
• Create donor awareness of potential hazards and administer donor consent forms
• Educate donors regarding general health assessments and counsel them about unacceptable test results
• Evaluate and manage donor injuries and adverse events
• Evaluate illness and medication histories to ensure continued donor suitability
• Assist with employee training and coaching regarding medical SOPs
• Administer the employee Hepatitis Vaccine program

Registered Nurse

• Perform physical examinations and establish medical histories to determine donor suitability.
• Build rapport with donors to ensure overall customer satisfaction.
• Ensure donor and staff confidentiality.
• Raise donor awareness of potential hazards.
• Provide donor education regarding general health and counsel donors regarding unacceptable test results.
• Evaluate and manage donor injuries and adverse events.
• Evaluate histories of illness or medications to ensure continued donor suitability.
• Assist in employee training.
• Administer the employee Hepatitis Vaccine program.

LPN/LVN

• Perform physical examinations and establish medical histories to determine donor suitability
• Build rapport with donors to ensure overall customer satisfaction
• Ensure donor and staff confidentiality
• Make donors aware of potential hazards
• Provide donor education regarding general health and counsel donors regarding unacceptable test results
• Evaluate and manage donor injuries and adverse events
• Evaluate illness and medication histories to ensure continued donor suitability
• Assist in employee training
• Administer the employee Hepatitis Vaccine program

EMT/LVN

Financial Planning and Analysis

• Assist the Global Innovation & R&D Controlling department with control and reporting for the Scientific Innovation Office
• Perform month-end close duties, including journal entries and management reports
• Understand ongoing R&D operations and the status of R&D projects
• Manage actuals versus budget to help R&D attain targets
• Oversee maintenance of R&D tracking systems and enhance project tracking capabilities
• Develop methodologies and execute processes to create meaningful data representations for R&D project tracking
• Perform business budgeting and forecasting
• Manage monthly and year-end closing and financial reporting processes
• Analyze operating results and budget-versus-actual reporting, including detailed variance explanations
• Provide support for special projects and ad hoc requests
• Prepare business cases and financial evaluations for pipeline projects and new business opportunities
• Assist in maintaining the cost accounting system, including master data and project portfolio

Senior Finance Analyst – R&D Controlling, BI

General

• Ensure current Good Manufacturing Practices (cGMP) and Health Canada/Grifols Quality Systems are followed during validation protocol performance, documentation, and review
• Travel to donor center sites to perform Operational Qualification/Performance Qualification testing
• Interact with Donor Center and Field Quality/Operations personnel to facilitate timely, documented validation approval
• Assist in keeping validation approaches current with regulatory expectations and industry standards
• Execute freezer installation, operational, and performance qualifications on-site
• Analyze validation data to ensure acceptance criteria are met and participate in writing validation summaries
• Communicate with Field Quality/Operations and Quality Assurance personnel regarding compliance and cGMP issues
• Write and execute test cases for critical control points, user requirements, and functional designs
• Prepare validation reports for distribution
• Ensure milestones and timelines are met on assigned projects
• Participate in evaluating processes, systems, and donor center equipment needs and final approval
• Prepare validation equipment for use and evaluation upon return
• Assist in identifying processes, systems, and equipment requiring addition, removal, or revalidation
• Track and monitor process/system failures and equipment calibration due dates and failures/events
• Provide feedback to Donor Center management on requirements, results, calibration, and validation processes
• Prepare donor center staff for validation activities and conduct training where applicable

Validation Specialist

Clinical Specialist

• Provide hands-on technical support for day-to-day clinical and manufacturing operations
• Perform patient molecular/serologic and manufacturing sample testing
• Perform and summarize data for review and reporting
• Monitor daily, weekly, and monthly quality control of equipment and systems
• Perform duties related to tests, instruments, and reagents; identify and escalate potential problems
• Maintain clean, organized laboratory and proper PPE/sample/material handling
• Log incoming materials and accession clinical samples in the Laboratory Information System (LIS)
• Transfer data accurately, generate electronic reports, document final results, and submit results for review
• Use LIS to sign off test completion and communicate results ready for review or release
• Report incorrect sample submissions and communicate written reports to clients
• Assist with training new employees and perform staff competency assessments
• Perform feasibility studies and assist in developing new assays
• Assist with strategic project testing and summarize data
• Participate in validation protocols and summarize validation data
• Perform annual equipment calibrations
• Use Microsoft tools to summarize quality metric data
• Support documentation of SOP deviations in MediaLab
• Enter deviations and CAPA submissions/updates in MediaLab
• Place online reagent and maintenance orders
• Maintain laboratory organization and appearance

Clinical Laboratory Specialist

Manager

• Evaluate processes, develop action plans, and coordinate strategic implementation of quality system processes and corrective actions at the plasma donor center
• Maintain oversight of the center’s quality management system and drive continuous quality improvement
• Direct and monitor processes for regulatory compliance and implement quality-control SOPs
• Oversee the center training program, training records, and staff competency
• Collaborate with the Center Manager to maintain product quality, donor suitability, and donor safety
• Manage personnel functions for the Quality Associate, including work assignment, hiring, development, training, discipline, termination, scheduling, and task follow-up
• Oversee internal and external audits, corrective/preventive actions, and follow-up
• Assess quality and training system effectiveness through trend recognition, failure investigation, and direct observation
• Document, investigate, and perform root-cause analysis for deviations and customer complaints
• Investigate trends and assess the effectiveness of corrective/preventive actions and process improvements
• Oversee product and biohazard waste shipments, labeling, documentation, and final shipment authorization
• Review unsuitable test results, unit lookback information, donor adverse event reports, and related documentation
• Ensure annual job and center training is completed and documented
• Conduct employee training observations before independent work release
• Verify supplies and materials meet quality requirements and are properly stored; investigate or reject non-conforming supplies
• Determine donor suitability, manage donor deferrals, and review deferred donor reinstatements
• Prepare quality analysis reports and research systemic compliance issues
• Ensure CLIA proficiency test surveys, complaint investigations, and training are documented
• Hold monthly Quality Meetings to communicate updates and manage action outcomes

Quality Manager

• Provide hands-on technical support for day-to-day clinical and manufacturing operations
• Perform patient molecular/serologic and manufacturing testing of samples
• Perform and summarize data for review and reporting
• Participate in method validations and validation protocols
• Monitor daily, weekly, and monthly QC of equipment and systems
• Identify instrument or reagent problems and escalate them to the Lead
• Maintain a clean and organized workplace
• Handle PPE, samples, and materials properly; log incoming materials
• Perform high-, mid-complexity, and simple routine tests
• Transfer data accurately, generate electronic reports, document final results, and submit results for review
• Accession clinical samples in the Laboratory Information System (LIS)
• Use LIS to sign off test completion and communicate results readiness to management
• Report incorrect sample submissions and communicate written reports to clients
• Assist with training new employees and perform staff competency assessments
• Adhere to SOPs, Quality System Essentials (QSE), cGMP, and regulatory guidelines
• Perform feasibility studies and assist in developing new assays
• Assist with strategic project testing and summarize data
• Perform annual equipment calibrations
• Use Microsoft tools to summarize quality metric data
• Support Leads by documenting SOP deviations in MediaLab
• Enter deviations and CAPA submissions/updates in MediaLab
• Maintain laboratory organization and appearance
• Place online reagent and maintenance orders using appropriate software systems

Senior Clinical Laboratory Specialist

Phlebotomist

• Assist in determining donor suitability
• Establish rapport with donors to ensure customer happiness while maintaining donor confidentiality
• Respond to and assist with donor reactions
• Monitor donors and equipment to ensure donor health and product quality
• Set up, disconnect and operate automated plasmapheresis machines
• Disconnect and dispose of contaminated disposable equipment
• Work in a plasma center while following required safety and protective-equipment procedures

• 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
• Provide donor awareness to potential hazards
• Provide donor education regarding general health and counseling regarding unacceptable test results
• Evaluate and manage donor injuries and adverse events
• Perform evaluations of illness history or medications to ensure continued donor suitability
• Assist in employee training
• Administer employee Hepatitis Vaccine program

LPN, LVN, RN

• Assist in determining the suitability of donors
• Establish rapport with donors to ensure customer happiness while maintaining donor confidentiality
• Respond to and assist with handling donor reactions
• Monitor donors and equipment to ensure donor health and product quality
• Set up, disconnect, and operate automated plasmapheresis machines
• Disconnect and dispose of contaminated disposable equipment

Processor

• Collect and process donor samples for processing and testing
• Record the weight of products and samples
• Label samples and freeze units for final packing within the required timeframe
• Pack units for final shipment
• Pack samples and prepare shipping boxes for shipment to the testing laboratory
• Monitor stored products
• Report equipment working conditions
• Maintain accurate donor files
• Handle shipping and inventory control responsibilities
• Maintain active communication and quality

Plasma Processor

• Assist in determining the suitability of donors
• Establish rapport with donors to ensure customer happiness while maintaining donor confidentiality
• Respond to and assist with handling donor reactions
• Monitor donors and equipment to ensure donor health and product quality
• Set up, disconnect, and operate automated plasmapheresis machines
• Disconnect and dispose of contaminated disposable equipment
• Work in a plasma center supporting Grifols’ plasma-derived medicines business

• Assist in determining the suitability of donors
• Establish rapport with donors to ensure customer happiness while maintaining donor confidentiality
• Respond to and assist with handling donor reactions
• Monitor donors and equipment to ensure donor health and product quality
• Set up, disconnect, and operate automated plasmapheresis machines
• Disconnect and dispose of contaminated disposable equipment
• Work in a plasma center with required personal protective equipment and exposure controls

• Assist in determining donor suitability
• Establish rapport with donors to ensure customer happiness and confidentiality
• Respond to and assist with donor reactions
• Monitor donors and equipment to ensure donor health and product quality
• Set up, disconnect, and operate automated plasmapheresis machines
• Disconnect and dispose of contaminated disposable equipment
• Work in a plasma center providing phlebotomy and donor-care services