R&D Hardware Innovation Specialist

11 hours ago


Glostrup, Glostrup Kommune, Denmark Agilent Technologies Full time
Job Description

We are seeking a R&D engineer to join our System Lifecycle Support team, which is part of Pathology R&D in our Diagnostics and Genomics Group.

The team's responsibilities include:

  • Instrument improvements projects/activities, such as feature enhancements and design optimizations based on customer feedback;
  • Instrument product care/sustaining activities;
  • Instrument design transfer projects (development and in-sourcing);
  • Design Control and design documentation.

Responsibilities:

As an R&D engineer, you will work with the team to drive activities and projects related to our instrument portfolio.

You will provide expert inputs during manufacturing issues, customer complaint handling, improvement projects, etc. Your input will have a direct impact on our ability to deliver to the market, user safety, and compliance with regulatory requirements.

To succeed, you will collaborate with various stakeholders within the organization, including Marketing, Procurement, Regulatory Affairs, Quality Assurance, Manufacturing, and Global Service.

Your tasks will include:

  • Planning and executing sustain activities;
  • Analyzing complaints with unknown root causes;
  • Securing good hardware design, serviceability, and manufacturability during instrument enhancement projects;
  • Ensuring that marketed instruments comply with regulatory requirements;
  • Planning and testing as part of verification;
  • Documenting according to internal and regulatory requirements.

Qualifications:

  • A background in Mechanical or Electrical Engineering, with experience in engineering design, product development, and sustaining/maintenance;
  • Experience with design and manufacturing of metal and plastic parts and knowledge on how to obtain robust product designs through product development;
  • Experience with design controls, including requirements engineering, design verification, change control, product risk management, and documentation, with medical devices;
  • Experience from a regulated environment – Medical Devices or Pharma;
  • Skills in robust engineering design and root cause analysis;
  • Proficiency in English, both written and spoken.


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