Grifols is a integral healthcare company that has been working since 1909 to improve health and well‑being worldwide. We are leaders in plasma‑derived medicines and transfusion medicine and develop, produce and market innovative medicines and services in more than 110 countries.Equal Employment OpportunityGrifols is an equal‑to‑opportunity employer and is committed to fostering an inclusive environment. Adjustments can be made for applicants with disabilities.Position OverviewThe QA Plasma Operations & Lookback Specialist will control and oversee the acceptance process for plasma and non‑plasma raw materials in accordance with established specifications to ensure compliance with legal, regulatory and customer requirements.ResponsibilitiesCoordinate the surveillance process for plasma unitsEnsure that the surveillance of plasma units alerted as post‑donation information are handled according to the approved proceduresEnsure compliance with the established deadlines in the management of alertsAnalyze the causes that give rise to communications and inform the Technical Management when the reason requires itEvaluate the potential risk of plasma batchesAnalyze the data and prepare periodic reports on the processOther administrative tasks related to the plasma surveillanceControl the acceptance process for raw materialsEvaluate the supplier documentation associated with the receipt of plasma shipments and plasma fractions against the approved requirementsAssess the maintenance of the cold chain during transportation in accordance with the specificationsReport and verify the results of the acceptance of plasma materials according to the approved inspection plans, making decisions regarding the use of the associated shipmentsManage discrepancies and potential deviations in the process with plasma suppliersEstablish and maintain guidelines to be followed in the purchasing and evaluation process of quality‑subjected suppliers, advising the coordination carried out by the Purchasing SectionData analysis, filing and administrative tasks related to the raw materials processCoordinate the workflows within the lifecycle of plasma fractions to ensure their availability within the established timelinesManage any deviations that occur and collaborate in the investigations that ariseContribute to the necessary tasks for the release of plasma fractions to customersData analysis, filing, and administrative tasks related to the management process of intermediate productsQualificationsBachelor's degree in Health Sciences (Pharmacy, Biology, Chemistry);
a Master’s or postgraduate degree in the pharmaceutical sector is valuable3 years of experience within Pharma QualityKnowledge in GMPBasic statistical knowledgeProficiency with MS Office and SAPAdvanced level of EnglishScheduleMonday to Friday, 14:00–22:00 (afternoon shift)Benefits PackagePermanent positionOccasionally remoteLocation: Parets del Vallès, Spain

📌 Qa Operations Specialist (Parets)
🏢 Grifols
📍 Parets