Principal Associate Qa - Idm (r3 – R4)

Eli Lilly Eli Lilly · Pharma · Indianapolis, IN

This role provides quality oversight for medical devices and combination products during technical transfer to contract manufacturing operations, ensuring design meets critical requirements and risks are identified and addressed. It also verifies equipment fitness for use and manufacturing readiness for contract manufacturers and suppliers.

What you'd actually do

  1. Provide quality oversight and support for medical devices and combination products during technical transfer to contract manufacturing operations.
  2. Ensure design meets critical requirements and risks to product quality have been identified, addressed in the design and tested.
  3. Verify that equipment is fit for use and ensure manufacturing readiness for prospective contract manufacturers (CM) and suppliers.
  4. Provide quality oversight for the technical transfer of medical devices in the emerging IDM portfolio.
  5. Support device development reviews to ensure appropriate design for manufacturability.

Skills

Required

  • Bachelor’s degree in Chemical Engineering, Mechanical Engineering, or a related field
  • 5 years of progressively responsible experience in Quality, Technical Services, Product Development, and/or Manufacturing of medical devices
  • 5 years of experience with global medical devices and combination product regulations (e.g. 21CFR820, 21CFR Part 4, Part 11, ISO 13485, ISO 11608, Canadian MDR, EU Medical Devices Directive/Regulation, JPAL, TGA, ANVISA)
  • 5 years of experience with Quality System elements, devices, design, manufacturing, and validation and their application in a manufacturing environment
  • 5 years of experience with plastic molding/assembly operations
  • 5 years of experience with Microsoft applications, Veeva, and TrackWise

What the JD emphasized

  • global medical devices and combination product regulations
  • Quality System elements, devices, design, manufacturing, and validation