Posted:1 week ago| Platform: Linkedin logo

Apply

Work Mode

On-site

Job Type

Full Time

Job Description

  • Preparation of CTD/eCTD format drug master file and its submission to various regulatory authorities including USA, Europe, Canada, Australia, China, Japan, Korea, Brazil and ROW market
  • Preparation of query response of drug substance for various and less regulated markets and customers.
  • Preparation of applicant part and closed part for various authorities for different customers.
  • Preparation of annual updates and amendment of drug master files US via ESG, ASMF via CESP, KDMF via MFDS Korea,
  • Preparation and submission of CEP applications and responses to EDQM via CESP.
  • Preparation of CEP LOA’s & LOA’s and declarations of various customers and authority.
  • To collect and evaluate scientific data for assessment and prepare regulatory submission for authorities and customers

Mock Interview

Practice Video Interview with JobPe AI

Start Job-Specific Interview
cta

Start Your Job Search Today

Browse through a variety of job opportunities tailored to your skills and preferences. Filter by location, experience, salary, and more to find your perfect fit.

Job Application AI Bot

Job Application AI Bot

Apply to 20+ Portals in one click

Download Now

Download the Mobile App

Instantly access job listings, apply easily, and track applications.

coding practice

Enhance Your Skills

Practice coding challenges to boost your skills

Start Practicing Now
Cadila Pharmaceuticals Limited logo
Cadila Pharmaceuticals Limited

Pharmaceuticals

Ahmedabad

RecommendedJobs for You

Gurugram, Haryana, India

Bhiwandi, Maharashtra, India

Noida, Uttar Pradesh