Job Details
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