Offres d’emploi Anlagebuchhalter in 80 100 en Temporaire, Durée Déterminée, Projet dans le secteur Biotechnologie & Pharmacie

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ITech Consult AG - Lucerne Und Region, Lucerne(il y a 3 heures)
Senior Software Engineer- C+/Python/Linux/Git/OOA/OOD Job Description: For our client, based in Lucerne region, we are looking for Senior Software Engineer with proven experience in C+ development. Tasks and Responsibilities: -Software Development within the Simulacrum Scrum Team, providing a hardware simulation and test environment for various Instrument Control Software projects. -Participate in...
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MBA - Basel, Bâle Ville(il y a 7 jours)
For our Global Pharmaceutical Client we are recruiting for a Clinical Documentation Compliance Manager who will oversee the adherence and compliance of TMF data according to Global Clinical Regulations. This position sits within the Clinical Document Governance and Management team and reports to the TMF Operational Excellent Head. Responsibilities: Responsible for monitoring of TMF process complia...
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MBA - Solothurn, Soleure(il y a 6 jours)
Specialist Associate Supplier Quality Engineer is needed to support remediation project with regards to new MDR regulations. Requirements: Management supplier's related Non-Conformities (NC's).Ensuring timeline of NC closure and adequacy of corrective action as well as audit proof documentation Management of supplier's related Corrective and Preventive Actions (CAPA's) Management of supplier's cha...
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MBA - Solothurn, Soleure(il y a 6 jours)
We are searching for a quality engineer to join a remediation project to support compliance with EU MDR requirements. Your role will involve collaboration with suppliers to obtain details for manufacturing process information, production risk, management processes. RESPONSIBILITIES: performing and supporting tasks related to the technical file remediation products to meet EU MDR requirements. meet...
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MBA - solothurn, Soleure(il y a 9 jours)
We have a new opportunity for a regulatory affairs expert with prior experience in medical devices to support the team in creation and maintenance of Technical Documentation for CE marked products (implants and instruments) according to with MDR compliance framework. Tasks: Support preparation of technical documentation and develop dossier documentation for submission to and review by Notified Bod...
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MBA - solothurn, Soleure(il y a 9 jours)
Global medical devices company is looking for an experienced Quality Project Manager to support MDR compliance execution work by acting as project manager for external supplier relations who has oversight on ongoing MDR compliance projects and drives completion of MDR. Tasks: - Support execution of project plan for MDR compliance business for 2019 - Lead and track completion of MDR drawing updates...
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