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
• Travel for training required

Registered Nurse, Bilingual in Spanish

• 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 education regarding general health
• Evaluate & manage donor injuries and adverse events

Registered Nurse, Bilingual in Spanish - Travel for Training Required

Operations

• The Operational Excellence Intern will have the opportunity to learn more project management methodology, lean manufacturing methodology, an overview of the manufacturing process/equipment, and reliability/sustainability initiatives for the site
• Generate comprehensive file of key equipment across all buildings and list of existing/future projects to provide framework for long term sustainability initiatives
• Generate template for project meeting meetings, project schedules, project presentations, and other project documents
• Upload presentations from trainings, create calendar of activities, tools and templates of Lean Manufacturing from websites and create central folders in shared drive
• Support Shutdown Activities during planning, execution and area release
• Compile all project information of GB projects into standard template for prioritization
• Organize Shutdown and various Project Teams folders and format of teams for better user access
• Work with Associate Director of Project Management to assist with meeting minutes, meeting follow-up and other project tasks as needed
• Work with Director of Operational Excellence to assist with other unplanned activities/projects as needed

Intern – Operational Excellence

Backend Engineer

• Receive training on new maintenance and calibration management software (SAP PM)
• Enter the manufacturing area to see the equipment running and learn about the manufacturing processes
• Enter paper based preventive and corrective equipment maintenance procedures into SAP
• Upload Equipment documentation into SAP
• Create standard operating procedures for SAP equipment management software

Intern, Manufacturing Technical Support – Equipment Maintenance

Engineer

• Lead the preparation, review, and execution of Validation Plans, Protocols, and Reports for Cleaning, Equipment, Steam Sterilisation, and Process Validation in accordance with cGMP and regulatory requirements.
• Review and assess change controls, evaluate impact to validated systems, and define appropriate validation and re‑qualification requirements.
• Represent the Validation function during internal and external regulatory inspections, including those conducted by HPRA and FDA.
• Generate, review, and approve validation documentation including User Requirement Specifications (URS), protocols, reports, and SOPs.
• Provide hands‑on execution and oversight of validation activities to ensure equipment cleaning and processes meet current GMP and industry standards.
• Maintain the Site Validation Master Plan (VMP) and associated Project VMPs, defining validation approaches, study requirements, requalification strategies, and frequencies.
• Execute and coordinate revalidation activities in line with change management and lifecycle requirements.
• Perform risk assessments, manage deviations, and ensure timely closure of CAPAs.
• Independently resolve complex technical challenges, applying sound scientific judgment and adaptability in a dynamic manufacturing environment.
• Collaborate cross‑functionally with Operations, Quality, Engineering, and Maintenance to lead qualification and validation efforts supporting site projects.
• Review and analyse validation data to verify adequacy, data integrity, and regulatory compliance.
• Perform additional validation‑related activities as assigned by the Manager or Director.
• Act as a delegated signatory for validation documentation, with appropriate qualification and authorization from the Validation Manager.

Cleaning Validation Engineer – Lead

QA Engineer

• Provide routine technical support for various tasks including documentation, training, compliance, product release, and scheduling
• Execute assignments of medium complexity
• Communicate effectively and promptly at all levels of the organization
• Follow cGMP and department safety practices

Quality Associate II – Quality Associate III, QA Release

Director

• Lead and manage pathogen safety strategies and studies for product development and lifecycle management.
• Act as Study Director or site responsible for internal and external pathogen safety studies in GLP and non-GLP environments.
• Oversee project planning, execution, budget control, and cross-functional coordination within multidisciplinary teams.
• Evaluate and interpret pathogen safety study results, reporting progress to project teams and R&D management.
• Prepare, review, and approve technical reports, risk assessments, and regulatory documentation supporting registration dossiers.
• Ensure full compliance with GMP, GLP/BPL, quality, safety, and environmental standards, and promote a strong safety culture.

Director, Pathogen Safety

Compliance

• Ensure regulatory compliance and support global market access for IVD products
• Develop and execute regulatory strategies
• Prepare and submit complex pre-market and post-market applications to FDA, EU Notified Bodies
• Manage communications with health agencies
• Collaborate with cross-functional teams
• Provide regulatory input throughout the product lifecycle
• Mentor junior colleagues
• Monitor evolving regulations to identify risks and implement mitigation plans

Regulatory Affairs Specialist 3 – Medical Device, IVD

Administration

• Przygotowywanie i składanie ofert (kompletowanie dokumentacji zgodnie z wytycznymi ustawy PZP)
• Wsparcie w bieżących sprawach związanych z przetargiem (przygotowywanie wniosków, wysyłanie informacji o otwarciu przetargu itp.)
• Kompletowanie całej dokumentacji przetargowej i umieszczanie jej w systemie IT
• Prowadzenie folderu dla każdego klienta z pełną dokumentacją (oferta przetargowa, umowa, protokoły instalacyjne, listy itp.)
• Przygotowywanie i sprawdzanie formalnej dokumentacji przetargowej – KRS, ZUS itp. (monitorowanie terminów ważności)
• Wysyłanie oraz monitorowanie zapytań do działu finansowego dotyczących depozytów, gwarancji bankowych, ubezpieczeń
• Wsparcie w przygotowywaniu i sprawdzaniu dowodów rzeczowych – monitorowanie terminów ważności
• Monitorowanie biuletynu w celu wyszukiwania ogłoszeń o nadchodzących przetargach
• Współpraca z działem administracji w procesie zakupowym (dotrzymywanie terminów, wsparcie w zakupach)
• Monitorowanie umów, podpisów, archiwizacja

Administratora ds. Przetargów Publicznych

Community Manager

• Planung und Umsetzung regionaler Dialog‑ und Community‑Marketing‑Maßnahmen , um neue Blut‑ und Plasmaspender:innen zu gewinnen und die regionale Sichtbarkeit unserer Spendezahlen nachhaltig zu steigern.
• Verantwortung für die aktive Spenderakquise über zielgerichtete Aktionen, Events, Promotion‑Formate und persönliche Direktansprache – sowohl vor Ort als auch im Rahmen mobiler Outreach‑Aktivitäten.
• Aufbau, Pflege und Steuerung regionaler Netzwerke und Kooperationen mit Unternehmen, Vereinen, Bildungseinrichtungen und weiteren regionalen Partnern, um langfristige Spenderpotenziale zu erschließen und Community‑Engagement zu fördern.
• Entwicklung und Durchführung regionaler Spenden‑ und Outreach‑Aktivitäten im Einklang mit zentralen Marketingleitlinien – inklusive kreativer Ansätzen zur Neuspendergewinnung, Reaktivierung und Steigerung der regionalen Sichtbarkeit.
• Analyse der Wirksamkeit aller durchgeführten Maßnahmen sowie Ableitung konkreter Optimierungsmaßnahmen zur Effizienzsteigerung unserer Outreach‑ und Marketingaktivitäten.
• Ausbau regionaler Blutspendetermine : Identifikation neuer Gemeinden, Firmen oder Vereine für externe Blutspendetermine sowie Bewertung bestehender Standorte
• Unterstützung der Spenderbindung und Reaktivierung bestehender Spender:innen durch persönliche, dialogorientierte Kommunikation – telefonisch, im direkten Austausch sowie über weitere geeignete Kanäle und Medien.
• Enge operative Zusammenarbeit mit Regionalleitung, Center Management und dem zentralen Marketing , um regionale Zielsetzungen optimal umzusetzen und eine einheitliche, professionelle Präsenz im Spenderkontakt sicherzustellen.

Dialogmarketing, Community Engagement Specialist

Human Resources

• Provides strategic client-focused support
• Implements business unit/departmental change
• Provides solutions to business issues
• Advocates sound principles of people management practices
• Manages employee relations issues
• Develops and maintains standard operating procedures (SOPs)

Human Resources Business Partner III

• Manage QA Documentation Department and systems
• Change Control Management and Document Management System
• Ensure that all changes to documents, facility computer and packaging components are properly documented, justified and approved
• Manage/supervise QA staff and ensure their growth/development through effective performance counseling and training
• Oversee and provide direction in the maintenance of the change control system and Document management system
• Review all change requests for clarity, purpose, justification and Regulatory requirements
• Prepare information for annual reportable changes to be submitted to FDA
• Routine reporting of document workflow status and upcoming/overdue procedures for periodic review
• Evaluate and implement process and system improvement
• Site representative as system owner for groups consisting of various Grifols sites for benchmarking and harmonization efforts
• Ensure that product impacted by change is placed on hold
• Responsible for design, development, revision of packaging and labeling
• Maintain effective communication with management
• Manage operational budget
• Chair all change boards
• Provide guidance and support to production on cGMP compliance
• Provide support, direction and coaching to subordinate employees in the areas of the QA department
• Participate in regulatory and internal inspections/ audits including providing written responses as applicable for area of responsibility.

Manager, Quality Assurance Documentation

Manager

• Acts as the general manager for a Plasma Collection Center and has overall responsibility for the center's operation.
• Works under general occasional guidance and general oversight of regional management.
• 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.
• 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.
• Provides strategic direction and planning.

Center Manager – Plasma Donation

• 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/LPN, Bilingual Preferred – Plasma Donation Center

Software Engineer

• Work independently to troubleshoot and provide sound technical and engineering solutions for complex equipment, process and control issues
• Locate/identify replacement parts, coordinate multiple and interdisciplinary work requests, and investigate equipment repair history using the CMMS
• Implement various projects. Define the scope, specifications, and work with vendors
• Support the commissioning and validation of the equipment and any Computerized Maintenance Management System requirements
• Develop and perform calibration on various types of process instrumentation and control elements
• Troubleshoot, coordinate schedules, and perform corrective maintenance on process instrumentation and control elements
• Provide detailed documentation of all calibration, troubleshooting, and repair activities.
• Issue/complete job hazard analysis/safe work permits (hot work, excavating, confined space, hazardous atmosphere, etc.)
• Use a Computerized Maintenance Management System to document work activity
• Adhere to cGMP, Safety and Environmental requirements
• Follow Standard Operating Procedures, Piping & Instrumentation Diagrams, job plans and/or equipment manuals to perform work
• Responsible for maintaining training curriculum requirements
• Develop and administer qualification requirements
• Assist with modification, installation and start up of new and existing instrumentation, process control systems and equipment
• Assume role of Lead Technician and Supervisor Designate
• Oversee contractor performance
• Train and mentor other technicians