Bjorn Legler
About
Bjorn Legler is from Copenhagen, Capital Region, Denmark. Bjorn works in the following industries: "Medical Equipment Manufacturing". Bjorn is currently Senior R&D Project Manager at Oticon Medical, located in Copenhagen, Capital Region, Denmark. In Bjorn's previous role as a Hardware Manager, R&D at Demant, Bjorn worked in Copenhagen Area, Capital Region, Denmark until Jan 2021. Prior to joining Demant, Bjorn was a Hardware Manager, R&D at Oticon and held the position of Hardware Manager, R&D at Copenhagen Area, Capital Region, Denmark. Prior to that, Bjorn was a Hardware Platform Architect at Oticon A/S, based in Copenhagen Area, Denmark from Oct 2014 to Feb 2018. Bjorn started working as Lead developer at Oticon A/S in Nov 2011. From Dec 2005 to Nov 2011, Bjorn was Development Engineer Electro-Acoustic System Design at Oticon A/S. Prior to that, Bjorn was a Intern at Etymotic Research, based in Elk Grove Village, Greater Chicago Area from Sep 2003 to Jan 2004.
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Bjorn Legler's current jobs
Product Project definition and activation End-to-end responsibility - from concept development to market introduction Delivering Medical Class III devices to the market according to the product road map Manage and lead development of product projects according to quality management system(s) Leading the Gate reviews ensuring the agreed performance level, quality, cost, and producibility Release platform documentation in compliance with FDA/MDR Stakeholder Management Supplier Management Managing project budget Contribute in the balancing and planning of the product portfolio
Bjorn Legler's past jobs
Accountable for high performing personnel Competence development for individual employees and strategic development of the group Technical Project Management Execute projects according to project briefs Plan & lead development project in accordance with QMS Supplier Management Delivery Accountable for Hearing Instrument Hardware Platforms to Product program Ensure agreed performance level, quality, cost, and producibility Release platform documentation in compliance with FDA/MDSAP Stakeholder Management
Accountable for high performing personnel Competence development Technical Project Management Delivery of Hardware Hearing Instrument Platforms Ensure agreed performance level, quality, cost, and producibility Release platform documentation in compliance with FDA/MDSAP
Architecture specifications Requirements specifications Cross functional alignment on system level Keep track on market trends Input for Technology and sub roadmap Initiate early concept studies Stimulate platform innovation Initiate core asset, concept and platform orders Input to product definition incl. product requirements
Technical project coordination for electro acoustic development Development lead on larger projects Owner of the technical overview and system configuration on a high level Configuration of platform and core assets for the project (framework for development work) Acoustic design, selection of components Platform calibration/setting Facilitate electro acoustic problemsolving, sparring for developers Process know-how and competence development within the group Prepare and drive design reviews and requirements Secure the quality of professional work Ensure Systems arcitecture throughout development projects Strong interface with other delivery groups Main competence interface to the Project Manager and Systems Managers
Transducers Electro acoustic development Product integration and configuration management Hearing aid testing Documentation Method & tool development Product development for production