02.05.24 | Vollzeit | Zug | Michael Page InternationalAnd maintenance of the LAB (as needed) - Creating documentation required to comply with established processes (as needed) - NOTE Depending on the experience and seniority level tasks can be extended with a focus on mechanical testing of packaging products such as auto-injectors or pen injectors The Successful
Später ansehen02.05.24 | Vollzeit | Schaffhausen | Randstad Schweiz AGAnd services to advance the health and well-being of people. Cilag AG is an international manufacturing company of the Janssen pharmaceutical division of the Johnson & Johnson Group and produces pharmaceutical and medical device products as well as active chemical ingredients (APIs) for global markets at its
Später ansehen29.04.24 | Vollzeit | Hays AGAnd internal subject matter experts to incorporate critical factors for absorption and DP-performance into formulation development strategy o Generate accurate and comprehensive scientific documentation, including development reports and manufacturing instructions, to support development trials, process
Später ansehen24.04.24 | Vollzeit | Sempach, Sempach Stadt | Randstad Schweiz AGFor our client specialized in Medical Device area, we're looking for a Product engineer administrator Location Lucern canton Position Permanent You will play a crucial role in maintaining and managing SAP basic data in the product engineering domain. You will be responsible for creating
Später ansehen16.04.24 | Vollzeit | Zug | AdeccoCertification or possess a relevant university degree in natural sciences. - A minimum of 1-3 years in quality control, medical laboratory diagnostics, or chemical testing. - Demonstrate a strong affinity for precise and accurate work, along with a commitment to maintaining high quality standards, applying good
Später ansehen28.03.24 | Vollzeit | Le Locle | Randstad Schweiz AGWe are currently seeking a Quality engineer for one of our clients in Canton of Neuchatel. If you are looking to work in a dynamic and very friendly working environment and in the medical devices sector then this is for you. This is an open ended temporary contract. Please note this vacancy
Später ansehen28.03.24 | Vollzeit | Lausanne | Randstad Schweiz AGCompliance/Quality system roles. - A Bachelor’s or Master’s degree in medical technology, life sciences, or a related field (or equivalent work experience). - Experience in documentation control and record management is preferred. - Excellent organizational, problem-solving, and interpersonal skills
Später ansehen04.12.23 | Vollzeit, Freelancer | Hays AGSubmission with CMOs o Revision of technical documentation o Managing operational activities for the variation submissions e.g uploads of documents, maintaining trackers, QC of submission packages o Compliance check of 32A1 part of the dossiers o Maintaining information in submission tracking systems Your
Später ansehen04.11.19 | Vollzeit | Zürich | Ava AGAs the best Swiss startup in 2017 and 2018. Our current key markets include USA, Germany, Switzerland and UK. Would you like to join us on our challenging adventure? Responsibilities - Develop clinical trials in women’s health from A to Z (e.g. trial design, statistical analysis plan, clinical documentation
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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