Support Jobs in Root
46 Jobangebote auf 6 unterschiedlichen Anzeigenmärkten gefunden.-
NCMR Coordinator - Quality Engineer
04.04.2024 Luzern, 6037, RootNovocure VollzeitTo support our team in Root, Switzerland we are looking for a NCMR Coordinator – Quality Engineer In this role as NCMR Coordinator you are responsible for the NCMR process. The NCMR coordinator is responsible for the review, management, and processing of the nonconformance reports generated in the Quality System, to address quality...
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Senior Linux System Engineer 80-100% - Remote First
23.11.2023 Bern, 3000Adfinis AG Vollzeitcomprehensive documentation and describe concepts in a concise way lead customer meetings and establish a constructive relationship with the customer provide comprehensive product and service support, solve high-priority and high-impact issues, replicate problems and identify root causes Requirements Must-Have Hard Skills You have...
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Director - Analytical Lifecycle Strategy
19.04.2024 Vaud, WaadtRandstad (Schweiz) AGStay updated with regulatory guidelines and industry best practices. Ensure all analytical methodologies meet current pharmacopeial and regulatory requirements. Support filing of dossier variations / updates. Draft / review response to queries and observation from Health Authorities. Provide support during inspections and audits.
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Parenterals Tech Transfer Manager
19.04.2024 Vaud, 1400, Yverdongloor&lang AGSupport the young team of Global External Manufacturing in this challenging corporate role! Your expertise: Subject matter expert (SME) in sterile manufacturing processes Support the process capability analysis and Continuous Process Verification of key quality attributes and parameters at the different CMOs Provide Impact
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Director Analytical Lifecycle Strategy (m/f/d)
04.04.2024 Vaud, 1262, EysinsFresenius Kabi SwissBioSim GmbHEnsure all analytical methodologies meet current pharmacopeial and regulatory requirements. Support filing of dossier variations / updates. Draft / review response to queries and observation from Health Authorities. Provide support during inspections and audits. Participate in analytical deviation and OOx investigation, root cause...
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Senior CAD Designer - Medical Device
06.03.2024 Basel Stadt, 4000, BaselNovartis Pharma GmbH VollzeitEnsure device design development is delivered to a high quality • Lead testing and characterization for acceptance, compliance, performance etc., and suggest improvements • Perform root cause analysis and develop robust solutions to prevent re-occurrence. Ensure components are delivered and controlled to the required quality for clinical trials and...
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Welding Engineer: General Support (EN-MME-FW-2024-78-GRAP)
17.04.2024 SchweizCERN Vollzeitmanufacturing and assembly of accelerator and detector devices.As a Welding Engineer in the Forming & Welding section (MME-FW), you will provide a general support for the welding activities in a highly technical environment with state-of-the-art equipment in CERN s main workshop.Your main tasks will be to:Participate to the preparation and the...
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Application Support Analyst - Ebanking
24.03.2024 SchweizBarclays Vollzeitbusiness continuity testing; and provision of 24x7 support. The role holder must ensure that all live applications are fully supported and meet the SLA requirements of service area. They will also effectively provide service acceptance measurement and sign off for their area of responsibility; manage and deliver second line application support whether direct,...
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Global Transport Management Supporter
19.04.2024 Bern, 3000Bavarian Nordic A/SR&D innovation, manufacturing, and commercialization. We aim to improve health and quality of life for children and adults around the world – protecting our tomorrow. We hope that you will share this mission with us. Transport Management Supporter – Identify and define the best product transport methods We are looking for a Transport Management Supporter, to
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Engineer Mfg Science Drug Substance / Johnson & Johnson
19.04.2024 Bern, 3000RandstadMain Responsibilities Writing GMP process documents like MBR, Work Instructions, Equipment manuals and Process Risk assessments Writing of electronical Batch Records will be one of the main tasks at the beginning Train Operators on written process documents Support PPQ (Process Performance Qualification) Managing of Quality Issues, Root
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GMP Officer (m/f/d)
19.04.2024 Basel Stadt, 4000, BaselLonzathe timely finalization of deviations, CAPAs and change requestsSupport the creation and handling of deviations including root-cause analysis and definition of CAPAs Support the creation, planning, and execution of CAPAs and change requestsExecute efficiency tests of CAPA measures Support Track & Trend analysis of...
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Scientific Software Engineer - Data Analysis (EP-SFT-2024-55-LD)
17.04.2024 SchweizCERNera.Guarantee top runtime performance of ROOT data analysis and processing components, also through the expression of parallelism in all forms, including the exploitation of hardware accelerators such as GPUs.Curate a simple and powerful programming model, supported by ergonomic interfaces, interoperable between the Python and C++
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Project Manager Electro Installation
14.04.2024 Bern, 3000Experis- 5-10 years of experience to work within GMP environment in Switzerland - Electrical installation background- Rock solid understanding of Swiss & EU regulations and standards for electrical installations in industrial environment------------------------------------------------------- Aim of the position: Manages Engineering Projects to support the
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HRBP Switzerland and Austria
14.04.2024 Vaud, 1196, GlandEssilorLuxotticareceive high quality of HR generalist support we are recruiting a HR Business Partner. This HR Business Partner will work closely with the business leaders of different entities in supporting the business and driving the HR agenda. Key to the role is the effective daily management of transactional HR activities alongside with more...
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CMC Technical Officer, Center for Vaccine Innovation and Access
11.04.2024 SchweizPATH Vollzeitsufficiency for optimization and scale-up of the manufacturing and analytical processes under Good Manufacturing Practices (GMP).Support regulatory submissions such as eCTD Modules 2.3 and 3, by authoring or coordinating the authorship of CMC content.Participate in process troubleshooting and identify root causes of
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