Quality Engineer

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