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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. The Quality Associate/Sr. Quality Associate Materials Evaluation Coordinator performs in the Packaging area as a Quality representative for sampling, auditing, and making Quality decisions. In this area, the Quality Associate/Sr. Quality Associate Materials Evaluation Coordinator audits unlabeled final container vials, media, syringes and finished product batches using designated ANSI sampling plans. Additionally, the Packaging Quality Associate/Sr. Quality Associate Materials Evaluation Coordinator responsibilities include: reserve sampling, post-pack identity sampling, packaging commodity verification and reconciliation, line clearance verification, and stability sample inspection. The Quality Associate/Sr. Quality Associate Materials Evaluation Coordinator inspects product final container reserve samples according to approved standard operating procedures. Decisions made by Quality Associate/Sr. Quality Associate Materials Evaluation Coordinators have major compliance and monetary implications for Grifols.