regulatory affairs

Candidate will be responsible for

- Regulatory analysis and report writing.

- Generation of regulatory documents during product development, research and analysis of FDA databases, regulatory submission writing (510(k), de novo).

-Candidate should be experienced in technical writing.

-Candidate should understand medical device development processes (quality systems regulation) and be familiar with documentation typically generated within the process (e.g. risk management file, literature search, clinical assessments).

(Please mention NCRJobs.in for reference)

Location : Jaipur

Address : Near To Jaipur Airport