Assistant Manager III - Quality Control

KEY ACCOUNTABILITIES

Testing and release

Performing timely analysis and release of raw material and other samples for Pharmaceuticals.

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

Performing analysis of market complaints, Stability, process validation samples, Cleaning Validation of Pharmaceuticals.

Good Laboratory Practice

Performing 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.

Arranging and observing Control 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, 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, spares, 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.

Education / Experience

Post Graduate in Science (Organic Chemistry )

10-14 years in chemical & instrumental testing laboratory with exposure to GMP, GLP.

Technical skills &

Competencies / Language

• Analytical ability
• Trouble shootings
• Co ordination
• Communication