Title: Executive - Analytical Development

Date: Nov 8, 2024

Location: Tandalja - R&D

Company: Sun Pharmaceutical Industries Ltd

Analysis and reporting of Analytical method validation, method verification and method transfer.
Calibration of instruments
Preparation of method transfer / co-validation intimation/ protocol/ report/ /waiver/certificate generated in laboratory.
Make availability of document package (Specification, STP and pre-validation reports and related follow-up as and when required.)
Make availability of Procurement of logistics for method validation / method transfer or batch analysis.
Timely query response with the help of section head and R & D Quality.
Oral / written communication with internal / external persons at the time of protocol & report etc. preparation.
Document submission for the product registration.
Training and development activities.
Maintain cleanliness and housekeeping of the working area.
Any other responsibilities assigned by Department head/Designee from time to time orally or in writing.
Preparation of Protocols/ Reports / Documents generated in Laboratory
Preparation of SOP
Online data, log books review on shop floor
Training and development to new analyst for analysis
Daily monitoring of laboratory activities for the compliance against GMP
Follow and maintaining GMP during analytical activities