1) Strong background in Technical Writing (in Pharma or BioTech or Medical Device Industry)

2) Experience in a Good Manufacturing Practices (GMP) or (cGMP) environment

3) Quality System records as minor/major Deviations, CAPA and Change Control Records.

4) Experience with Device assembly and Packaging of final product - is a PLUS

5) Good documentation & communication skills

6) Exposure to KNEAT CDOCs - is Highly desired