KEY ACCOUNTABILITIES 

Testing and release 

Planning of timely sampling and analysis and review of raw material, bulk product, intermediates, finished goods, packing material and other samples for Pharmaceuticals.  

Performing analysis of Raw Material Samples received from new vendors for Pharmaceuticals. 

Good Laboratory Practice 

Planning for calibration & maintenance of lab. Equipment and assisting for the qualification of laboratory equipment. 

Reviewing pharmacopeias for specification preparation.  

Preparing SOPs and Formats and Analytical Test Record. 

Managing reference standards, working standards, laboratory reagents & chemicals. 

Reviewing and observing Retention Samples and maintaining record. 

Investigating out of specification results, retesting and review the analysis records. 

Maintaining & reviewing laboratory raw data related to testing activity. 

Validation 

 Preparing protocol for Analytical Method validation/Transfer, cleaning validation and performing the validation exercise as per the protocol. 

Management of laboratory Consumables 

Identifying and planning requirement for laboratory consumables and monitoring the stock of chemical, glassware and printed material. 

Co ordination 

Coordinating with production, and warehouse for analytical activities. 

Other  

Compliance to HSE Requirements for QC laboratory. 

Identifying and correcting unsafe conditions or behaviors and promptly reporting other potentially hazardous situations. 

Carrying out any other assignments or projects as per the instruction of the Dept. Head to meet with the organizational objectives and priorities.