Descripción de la oferta
Job DescriptionSandoz continues to go through an exciting and transformative period as a global leader and pioneering provider of sustainable Biosimilar and Generic medicines. As we continue down this new and ambitious path, unique opportunities will present themselves, both professionally and personally. As part of our Quality team you will manage quality aspects and projects within area of responsibility. You will also ensure and support overall GxP conformity and Compliance with the Sandoz Quality Management Systems.ResponsibilitiesOversight of all production and testing activities, ensures compliance with cGxP, incl. data integrity and eCompliance Support exception investigationsReview and approval of production, QC, and AS and T recordsMBR reviewExecutes batch release in compliance with registrationReporting of technical complaints / adverse events / special case scenarios related to Sandoz products within 24 hours of receiptDistribution of marketing samples (where applicable)Key Performance IndicatorsOn-time and GMP-compliant release of dosage formsNo complaints about inspections by authorities in your own area of responsibility without these being noticed and communicated beforehandSuccessfully support continuous improvement projectsExecutes batch release in compliance with registrationQualificationsQC/ QA in pharmaceutical industry / biotech with environmental monitoring.Collaborating across boundaries.Cleanliness zones.Continuous Learning.Dealing with Ambiguity.GMP Procedures.QA (Quality Assurance).Quality Control (QC) Testing.Quality Standards.Self-Awareness.Technological Expertise.Technological Intelligence.English – fluent reading and speaking.
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