Job Detail

Lead expert app development

Inseriert am: 02.06.2020

Nemensis ag Lead expert app development    Senden

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Standort: Schweiz, Basel-Stadt, Basel
Datum: 02/06/2020
Branche: Pharma-Industrie
Bereich: Technologie/EDV
Niederlassung: Reinach , Kägenstrasse 18
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For our client, an international pharmaceutical company in Basel, we are in search for a Lead Expert App Development (m/f/d) 100%. 


 


What the company offers you:



  • You will work as 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 company's Packaging & Device Development Team

  • Large and diverse infrastructure

  • Competitive salary

  • 1-year contract with a possibility of extension


 


Your responsibilities:



  • Taking technical leadership for the software development of mobile and/or web applications classified as SaMD

  • Providing software/systems life cycle expertise within a broader cross‐functional drug product development team

  • Supporting the standardization of the entire SaMD life cycle management process to utilize cross‐product synergies

  • Leading and/or supporting cross functional project teams during development, review and submission of regulatory dossiers

  • Leading risk management activities

  • Planning and monitoring of design verification activities

  • Supporting the improvement of the SaMD QMS


 


Your profile:



  • MSc/MA in computer science or relevant field and excellent understanding of the current Agile development methods and technologies

  • Experience in project / program management of complex projects

  • Autonomous and independent working style with at least 7 years of experience as technical, project management of projects with safety critical applications in a regulated environment

  • Experience in designing innovative software and systems architectures

  • Understanding of medical device regulations (FDA 21CFR 820, FDA 21CFR Part 4, EU Medical Device Directive, EU Medical Device Regulation), including those related to medical software (IEC 62304)

  • Fluency in English language incl. technical writing Experience desired; Proficiency in German


 


Welcome to nemensis!


We look forward to getting to know you!


 


Your contact person: 


Michel Vogt | Recruiter
Mail: michel.vogt@nemensis.com


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