Hi All!
I am willing to pursue a career as a regulatory
professional in the field of the medical device. I am RAC (US) certified and
completed required regulatory affairs courses from University of California,
San Diego. I don’t have direct hand on experiences in the medical device field.
I got an impression that potential employers in this field, mostly look for in
hand experiences in 510K submission and eCTD submission. I am currently
looking for a Mentor, an experienced professional like you, who can provide me
training in this area. Your tutelage will be invaluable for me. I can also
volunteer in your important regulatory document submission/archiving as needed.
At the end of training, I would request you to be one of the referees in my job
application and attest my capabilities.
I look
forward to have a positive response from you.
With best regards,
Jayanta Mukhopadhyaya
San Diego, California