19.04.24 | Vollzeit | Chur | NonStop Consulting | CHF 80’000 - CHF 85’000 / Jahr pharmaceuticals, beverages, and specialty products, contributing to a brighter future. The Role - You are responsible for checking feasibility, preparing quotations and documentation in accordance with customer requests. - You ensure timely order processing in terms of adherence to deadlines, quality and costs
Später ansehen25.04.24 | Vollzeit | Sort-en-Chalosse, Luzern | Michael Page InternationalProject Engineer Facilities Management Strategies (m/f/d) Luzern Interim - Job speichern - Aktualisiert am 19/04/2024 - International Pharmaceutical company - German and English needed Firmenprofil For our client, a leading international pharmaceutical company with modern offices in the canton
Später ansehen17.04.24 | Vollzeit | Basel (Basel-Stadt) | ACHIEVA Group Limited | CHF 72 / Stunde Assessments Being an expert and first level support for relevant quality systems (e.g. Cornerstone, Veeva OneQMS, QualityDocs, QRM,) Managing changes and deviations, as well as corrective and preventive actions in consultation with QA Provide expert support to monitor, update, and adapt the GMPrelevant
Später ansehen22.03.24 | Vollzeit | Luzern, Schaffhausen, Zürich | Daiichi Sankyo Europe GmbHImplementation are conducted within the electronic quality management systems in a timely manner Support all aspects of pharmacovigilance regulatory inspections including preparation, conduct, coordinating responses, evaluating supporting documentation, tracking and verification of CAPA commitment implementation
Später ansehen22.03.24 | Vollzeit | Zug, Dietikon, Kriens, Luzern | Daiichi Sankyo Europe GmbHImplementation are conducted within the electronic quality management systems in a timely manner Support all aspects of pharmacovigilance regulatory inspections including preparation, conduct, coordinating responses, evaluating supporting documentation, tracking and verification of CAPA commitment implementation
Später ansehen22.03.24 | Vollzeit | Zug, Schaffhausen, Zürich, Luz | Daiichi Sankyo Europe GmbHImplementation are conducted within the electronic quality management systems in a timely manner Support all aspects of pharmacovigilance regulatory inspections including preparation, conduct, coordinating responses, evaluating supporting documentation, tracking and verification of CAPA commitment implementation
Später ansehen22.03.24 | Vollzeit | Zürich, Schaffhausen, Luzern | Daiichi Sankyo Europe GmbHImplementation are conducted within the electronic quality management systems in a timely manner Support all aspects of pharmacovigilance regulatory inspections including preparation, conduct, coordinating responses, evaluating supporting documentation, tracking and verification of CAPA commitment implementation
Später ansehen22.03.24 | Vollzeit | Emmen, Uster, Dübendorf, Fraue | Daiichi Sankyo Europe GmbHImplementation are conducted within the electronic quality management systems in a timely manner Support all aspects of pharmacovigilance regulatory inspections including preparation, conduct, coordinating responses, evaluating supporting documentation, tracking and verification of CAPA commitment implementation
Später ansehen22.03.24 | Vollzeit | Dübendorf, Frauenfeld, Emmen | Daiichi Sankyo Europe GmbHImplementation are conducted within the electronic quality management systems in a timely manner Support all aspects of pharmacovigilance regulatory inspections including preparation, conduct, coordinating responses, evaluating supporting documentation, tracking and verification of CAPA commitment implementation
Später ansehen22.03.24 | Vollzeit | Schaffhausen, Zürich, Luzern | Daiichi Sankyo Europe GmbHImplementation are conducted within the electronic quality management systems in a timely manner Support all aspects of pharmacovigilance regulatory inspections including preparation, conduct, coordinating responses, evaluating supporting documentation, tracking and verification of CAPA commitment implementation
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