Executive - Quality Control

KEY ACCOUNTABILITIES

Testing and release

P lanning 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

P lanning 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.

Reviewi ng 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

Compli ance 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.