ASolution Pharmaceuticals Pvt. Ltd is hiring for Regulatory affair department

Details are mention below:

Experience Required : 3 to 8 yrs

Profile: 

* Preparation/compilation and submission of API (Active Pharmaceutical ingredient) and Drug Master File to Regulated market (US & Europe) 

* Evaluation of Product Development Report (PDR). 

* API/Bulk drug DMF Preparation and submission experience is must. 

* Preparation & Submission of DMF / COS in CTD & eCTD Format for all product as per requirement of regulatory authorities: Module 1, Module 2, Module 3

* Compliance of queries related to DMF/COS. 

* Compliance report of various audits by outside agencies & customer.

interested candidate can share profile on hr@asolution.in

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