Quality Engineer

2 weeks ago


Covington, United States Katalyst Healthcares and Life Sciences Full time
Responsibilities:
  • This individual will come from a Medical Device background with strong experience in quality engineering.
  • This consultant will be expected to be capable of writing procedures for the client independantly.
  • This person should have experience with FMEAs, and be comfortable with tasking on documents for risk management.
  • This consultant with be supporting Company, investigations, deviations, and CAPAs.
  • This person should have strong experience working within the Quality System and be proficient in technical writing and documentation skills supporting a medical device company.
Requirements:
  • Medical Device (4+ years)
  • Quality Engineering
  • Technical Writing
  • FMEA

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