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OPERATIONS - ENGINEERING/PRODUCTION
Photonics Design Engineer
Permanent contract
Full time
For our client active in medical devices and situated in region Ghent, we are looking for a Photonics Design Engineer who will be working on the optical part of CGM (continuous glucose monitor) and will be focusing on continuously improving the Silicon photonic IC and all related aspects.
Your main tasks and responsibilities include:
Design and simulate silicon photonic components and circuitsPropose and implement design solutions to meet systems requirementsMaintain and continuously improve our’s PDK (process design kit)Layout photonic ICs (GDSII format), tape-out to fabs and follow-upImplement test plans and analyse measurement dataConduct yield analysis to provide feedback for design optimizationDevelop and optimize new photonic modules (front-end, back-end, active/passive integration, packaging)Work on integration of lasers and photodetectors, both design and technology developmentInterface with internal and external teams for fabrication, assembly, packaging and testingWork cross-functionally and as part of the project team to incorporate the photonics expertise and have the ability, to adapt own work in the interest of the overall project
Life sciences
Your profile:
2+ years of industry experience in Silicon photonicsPhD in photonics or electronicsExperience in development of passive optical devices (waveguides, splitters, gratings, mux/demux, …)Strong knowledge photonic simulation and layout software (Lumerical, Fimmwave, IPKISS, Python, …)Experience with III-V integration on Silicon is a plus (flip-chip, bonding, transfer-print)An enthusiastic team-player, able to work cross-functionally and within project teamsWilling to work in a fast changing and challenging environmentPrior work experience in a start-up is a plusStrong written and oral communication skills – working language is EnglishAbility to write clear and comprehensive documentationAccept and be able to work in a medical device environment and be familiar with quality and regulatory standards for quality assurance, risk management, and others applicable to active implantable medical devices (e.g. ISO 13485)Clean Room & General Laboratory (Safety) training
Europe, Belgium, Flanders, East Flanders
8. Doctoral Degree (PhD)
1 to 3 years