Principal Scientist – design control of medical devices

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Can you take lead in projects and set the future standards for design control?

If you excel across design control and device development and you are looking for an opportunity to unfold all of your skills in a job with extraordinary influence and impact, you have found it. As part of LEO Pharma’s quest for becoming the world’s preferred dermatology care partner we want to develop new, innovative medical devices. We have a good basic foundation, full support from top management and exciting projects in our pipeline but we need you to help us take the next leap forward.

Development projects, new standards, audits…

Your overall focus is to contribute to the development of injectable treatments with user friendly and differentiated injection solutions based on thorough user and stakeholder understanding. As Principal Scientist you will act as spear head and set the future standards for design control within the device area in LEO. You will:

  • Act as design control spearhead and primary expert across device development projects. e.g. needle free injections
  • Set the overall direction for design control within device development in LEO
  • Act as design control specialist during audits
  • Ensure uncompromised focus on product requirements vs. manufacturing capability
  • Ensure compliance to relevant regulatory requirements
  • Ensure internal documentation compliance


  • You will unfold your skills across production methods and technologies, assembly techniques, product functionality and testing of critical quality attributes. As you will join an organisation in transformation you must thrive in a world of on-going changes – and have the ability to making business critical decisions when facing multiple opportunities.

    Design control experience and motivation for teamwork and knowledge sharing

    We are looking for a profile with drive and motivation for taking lead – with an additional open minded and positive approach that supports knowledge sharing and teamwork. As you will set our future standards for design control you must be able to communicate clearly and based on facts. As part of this you can define “Why, What and How” in a way that makes sense to authorities as well as colleagues and partners. Additionally your CV comprises:

  • A university degree in Engineering or related
  • 8+ years’ experience within design control related to development of medical devices
  • Extensive knowledge of FDA and EMA requirements for injection devices
  • Project management/coordination experience


  • Information og data

    Denne ledige stilling har jobtypen "Forsker", og befinder sig i kategorien "Sundhed og forskning".

    Arbejdsstedet er beliggende i Ballerup.

    Jobbet er oprettet på vores service den 13.1.2020, men kan have været deaktiveret og genaktiveret igen.

    Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
    • Forsker
    • Ballerup
    • Mandag den 03. februar 2020

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