Executive - Regulatory Affairs
4 - 8 Years of Experience
Not disclosed 
Full TimeSymbiotec Pharmalab Limited
Indore, Madhya Pradesh, India
Posted on 20-12-2021
2 Vacancies
Description
- Preparation and submission of Drug Master File (Module 2 and Module 3) and certificate of suitability applications for Active Pharmaceutical Ingredients for submission to European, USFDA and Rest – Of – World regulatory authorities.
- To ensure that all products are designed and developed in a way taking into account of cGMP and GLP.
- CTD Modules Preparation
- Compilation QOS
- API regulatory affairs.
- CTD Modules Preparation (Chemistry , Manufacturing and Control)
Category
Pharmaceuticals
Functional Area
Regulatory Affairs / Pharmacovigilance
Aggregated job.
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