QC Lab Technician (80-100%) - befristet
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Description du poste
Ophtapharm AG is a certified producer in the ophthalmic field. Join our dynamic team and contribute to high-quality products! Tasks Conduct and document release analytics for raw materials and products. Perform analytical testing for deviations and troubleshooting results. Create and maintain SOPs and support lab process optimization. Skills Chemistry lab technician or similar qualification with GMP experience. Experience in instrumental analytics, especially HPLC. Proficient in GMP documentation and data integrity. Ophtapharm AG is an FDA/EU-GMP certified manufacturer in the pharmaceutical sector (ophthalmics). At our production site in Hettlingen near Winterthur, high-quality products such as eye drops, ointments, and gels are aseptically produced, filled, and packaged for international markets. QC Lab Technician (80-100%) - fixed-term The QC Finished Products team ensures the quality of our raw materials, intermediates, and finished products through analytical testing under GMP conditions and plays a central role in handling deviations as well as in analytical troubleshooting. You can expect a varied laboratory environment with direct influence on the quality of our sterile products. For our team, we are looking for a conscientious and hands-on personality with solid practical experience in GMP-compliant release analytics as well as in handling deviations and OOS results. Your role Performing and documenting release analytics for raw materials, intermediates, and finished products according to GMP Analytical testing in the context of deviations, OOS results, and troubleshooting Handling and documenting deviations and OOS according to GMP requirements Creating and maintaining SOPs as well as supporting the optimisation of laboratory processes Qualification and requalification of laboratory equipment including GMP-compliant documentation Your profile Training as a chemical laboratory technician or comparable qualification with experience in a GMP environment Solid practical experience in instrumental analytics (especially HPLC, ideally complemented by other methods) Confident handling of GMP documentation and good understanding of data integrity Experience in handling deviations and OOS results Very good German and good English skills What’s more Working in a GMP-regulated environment with direct reference to sterile production Varied analytics with insight into troubleshooting and deviation handling Short decision-making paths and an uncomplicated team Good accessibility (public transport within walking distance) as well as free parking spaces Fixed-term position (1 year) with option for extension For personnel service providers: Unfortunately not this time. But we know where to find you if that changes. Do you have questions? HR Hettlingen, Human Resources, will be happy to answer them. Tel: +41 52 304 13 23.
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