Descripción de la oferta
Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? 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.Por favor, asegúrese de leer completamente el resumen y los requisitos de esta oportunidad de empleo que se detallan a continuación. We believe that diversity adds value to our business, our teams, and our culture. We are committed to equal employment opportunities, fostering an inclusive environment where diversity makes us outstanding. Mission From Quality Assurance we are looking for a Corporate Quality Auditor who will be the responsible to perform the Corporate Quality audits to the companies of Grifols Industrial group and affiliates, in order to evaluate and ensure the compliance of Good Distribution Practices, internal procedures and internal policies as well as to detect opportunities for improvement and best practices. Audits will be performed to Biopharma, Diagnostic and Healthcare busines units manufacturing sites (Pharmaceutical products and Medical Devices) and Grifols Affiliates. What Your Responsibilities Will Be Collect and review all documentation required to prepare and execute audit activities. Define and coordinate the audit agenda, ensuring alignment with audit objectives and stakeholders. Prepare all audit-related documentation prior to audit execution, including checklists, working papers, and supporting materials. Conduct Corporate Quality Audits, ensuring compliance with the approved audit plan, scope, and timelines. Prepare comprehensive audit reports, clearly documenting activities performed, identified risks, findings, and opportunities for improvement in a timely manner. Evaluate, classify, and document audit findings according to established quality standards, providing practical recommendations for improvement. Follow up on corrective and preventive actions (CAPAs) derived from audits, monitoring implementation and effectiveness. Support the management, monitoring, and reporting of quality indicators and key performance metrics within the area. Collaborate with internal stakeholders to promote continuous improvement and compliance across the organization. Ensure adherence to corporate quality standards, regulatory requirements, and internal procedures throughout the audit process. Who You Are You have a Life Sciences Degree (Pharmacy, Biology, Chemistry, Biotechnology) or Engineering Degree (Chemical or Industrial) or 10 years experience. You have 3-5 years of experience in GDP within pharmaceutical industry. High valuable to have experience in Auditing GxP. Strong analytical and communication skills. Availability to travel approximately 30%. Advanced English level, both written and spoken. What We Offer It is a brilliant opportunity for you, Grifols is fully aware that its employees are one of its major assets. We are committed to maintaining an atmosphere that encourages all our employees to develop their professional careers in an excellent working environment. Information about Grifols is available at We believe in diverse talent and want to remove any barriers that may hinder your participation. Grifols is an equal opportunity employer. Flexibility for U Program: Hybrid Model Flexible schedule: Monday-Thursday 7-10 to 16-19h and Friday 8-15h. (with the same flexible start time). xkdbapo Benefits Package Contract of Employment: Permanent position Location: Sant Cugat del Vallès. Location: SPAIN : España : Sant Cugat del Valles:[[cust_building]] Learn more about Grifols #J-18808-Ljbffr
