Altran AG jobs

Systems Engineer Aerospace

 Our OfferAltran is a global engineering consultancy and leader in R&D Services (ER&D), offering its clients a new way to innovate by developing products and services of tomorrow. The Altran Group provides its expertise to key players in the Aerospace, Automotive, Defense, Energy, Finance, Life Sciences, Railway, and IT/Telecom/Banking sectors, among others.The Global Industry Team in Zurich is looking for qualified and passionate systems engineer supporting our project requirements w...

Traction Control Engineer

 Our OfferAltran is a global engineering consultancy and leader in R&D Services (ER&D), offering its clients a new way to innovate by developing products and services of tomorrow. The Altran Group provides its expertise to key players in the Aerospace, Automotive, Defense, Energy, Finance, Life Sciences, Railway, and IT/Telecom/Banking sectors, among others. We are increasing our electrical engineering capabilities in Zurich and are therefore looking for passionate and hands-on engine...

Senior Stress Engineer

 Our OfferAltran is a global engineering consultancy and leader in R&D Services (ER&D), offering its clients a new way to innovate by developing products and services of tomorrow. The Altran Group provides its expertise to key players in the Aerospace, Automotive, Defense, Energy, Finance, Life Sciences, Railway, and IT/Telecom/Banking sectors, among others.We are looking to increase our local aviation engineering team based in central Switzerland with an additional stress engineer wh...

Human Factors Engineer

 To support the internal capabilities within the development team, we are seeking an experienced Human Factors Engineer to lead and monitor human factors activities in development of established and novel software as medical device (SaMD), drug delivery devices and combination products. This includes early concept phase work, formative evaluations to summative human factors evaluation.  Your responsibilities: Develop or implement human performance research, investigation, or analysis protocol...

System Engineer / Software Architect

 You would be creating products, tools and services that help enterprises manage their devices providing their employees with access to corporate applications, data and resources from virtually anywhere, on platforms such as Windows, iOS, Android and others, all while helping to keep corporate information and assets secure against known and emerging cyber threats meeting all the regulatory and compliance requirements. You will contribute to the development of software as medical device (SaMD)...

Analytical Expert

 Major Accountabilities: Previous experience working within the Life Science industryResponsible for the analytical support and developmentDrug development and quality control related projects in the area of analytical chemistryMethod development and validation for (U)HPLC, LC-MS, GC, GC-MS, IC, TitrationsGMP release of raw materials and intermediate Skills and expertise:GMPHPLCValidationSoPChange ControlQuality System / Quality ControlFDAAnalytical TechniquesProject Management Requirements: ...

Medical Device Regulatory Affairs Manager

 ResponsibilitiesDevelop, implement, communicate, and maintain global regulatory strategies and plans for devicesIdentify and communicate relevant guidance, policies, standards, and regulationsAssist the review of product and process documentation for assigned projects to ensure compliance with change control requirements to aid in determining if regulatory submissions are requiredCreation, review and maintenance of regulatory related technical documentationWork with cross-functional teams to...

CAPEX Project Manager

 ResponsibilitiesManage capital projects from basic design to execution and qualification/validation and deliver on time, within budget and according to defined specificationsEnsure the required quality, regulations and guidelines complianceBuild, coordinate and manage the project teams, cross functional, local or regionalManage all project -related documentation such as qualification (“DQ, IQ, OQ, PQ”) and requirement specificationsPerform project controls for cost and schedule according to ...

Senior Pharmaceutical QA Manager

ResponsibilitiesEnsure the pharma unit maintains the highest quality standards and are compliant with all regulations/procedures by driving continuous improvement activities Provide Quality guidance and support for investigations and change controlsDrive, lead and troubleshoot quality investigations to ensure that all critical and major quality issues are thoroughly investigated with appropriate corrective actionsInitiate improvements to the Quality Management System, ensuring compliance to a...

Software as Medical Device (SaMD Expert)

 In order to support the expanding development of "Software as a Medical Device" (SaMD), we are looking for a Lead Expert App Development. The successful candidate is a recognized expert for development and maintenance of safety critical mobile and/or web applications and will take over the technical leadership for the software development part for projects classified as SaMD within the Team.  Tasks and responsibilities will typically include:- Technical leadership for the software developmen...

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