24.04.24 | Vollzeit | Bern | NonStop Consulting | And U qualification requirements with suppliers and third parties. - You will revise technical documentation (P and IDs, technical specifications, spare lists) and write SAT protocols. - You will provide ongoing technical support for change control, deviation investigations, and CAPA management. - You
Später ansehen24.04.24 | Vollzeit | Gümligen | Randstad Schweiz AGUnd anspruchsvolle Gaseanwendungen für den industriellen und medizinischen Einsatz. Per sofort oder nach Vereinbarung stellen wir einen engagierten und motivierten SAP-Spezialisten ein - gesucht wird Technical SAP Specialist für Projekte & Support - langfristig temporär Zu deinen Aufgaben zählen - Pflege
Später ansehen18.04.24 | Vollzeit | Bern | Randstad Schweiz AGRefractometry, Manual titrations, Conductivity, .) - Being responsible for raw material sampling, when the need arises - Write scientifically-sound technical documents and reports - Support laboratory management, e.g., planning activities covering end-to-end raw materials process - Support a timely
Später ansehen09.04.24 | Vollzeit | Biel/Bienne | Swatch StoreVulnerabilities and automate repeatable tasks In this role, you will design, configure and migrate security infrastructures while developing and updating technical documentation. You will provide 3rd level support as a service Manager as well as on-call service on a weekly rotation basis. Last but surely
Später ansehen04.04.24 | Vollzeit, Studentenjobs | Konolfingen | Randstad Schweiz AGData Specialist ? Trial Management System 20% Activity rate hourly based We are currently seeking a data specialist - trial management system (20%) for our customer, Nestlé Research Center & Development Center in Konolfingen. The position is available starting from July or August 2024
Später ansehen26.03.24 | Vollzeit | Bern | Randstad Schweiz AGFor our client, a pharmaceutical company based in Bern, we are seeking a highly skilled Sr Engineer Projects Automation. The aim of this role is to manage Engineering Projects to support the development and manufacture of Pharmaceuticals in a regulated environment and maximize the benefit
Später ansehen31.10.19 | Vollzeit | Bern | Decomplix' ISO 13485 quality management system. - supporting our customers in quality management. - customer support on their regulatory path (pre- and post-market). - project management to bring the technical documentation of customer products to the point where they can obtain the CE mark for medical devices
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