5 development Jobs in Waadt gefunden.

Key Accountabilities Developing and modifying artworks for printed packaging components, including boxes, labels, leaflets, and foils, based on requests in the artwork management system, technical drawings, graphic guidelines, standard procedures, technical guidelines, and work instructions Ensuring that all artwork executions and corrections fully comply with expectations and applicable requirements Communicating completed

Johnson & Johnson AG in Zug is a leading sales and marketing organization in the medical sector. Our broad range of innovative products and service solutions caters to various stakeholders in hospitals and clinics.From industry-standard sutures, hemostats, mechanical stapling devices, and advanced energy products to comprehensive solutions for healthcare providers and decision-makers: for nearly a century, Johnson & Johnson Surgery has been focused on

YOUR ROLEWithin the Drug Substance Development (DSD) - Manufacturing department, we are looking for a "DSP Manufacturing Senior Technician " who will support the DSP large-scale operations (GMP and pilot).You will be part of a team of technicians, engineers and scientists specialized in the production and purification of recombinant proteins produced from animal cells.You will support the DSP activities from an operational and documentation point of view:

Your key responsibilities in this role are:Conduct routine analytical testing, method qualification execution as well as stability in an independent manner on:Liquid chromatography (PA, SEC, RP,…)Capillary Electrophoresis (icIEF, CGE-SDS)Able to validate/qualify analytical methods (LC, CE especially, but knowledge of OD, LC-MS, ELISA can be an asset)in GMP environmentDeliver data treatment/elaboration and analytical reports of

Independently conduct routine analytical testing, method qualification, and stability in a GMP environment in icIEF and/or CGE-SDS)Deliver high-quality data treatment and analytical reports in a digitally agile manner.Interact with customers to discuss results or coordinate routine and validation activities.Work autonomously on routine/non-routine activities requiring specialized technical expertise (e.g., stability).Strong expertise in GMP environment;