KEY ACCOUNTABILITIES

Performing timely analysis of raw material, bulk product, intermediates, finished goods and other samples for Pharmaceuticals.

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

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.

Participating in Investigation of out of specification results, retesting and review the analysis records.

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

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

Coordinating with production, and warehouse for analytical activities.

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.     

REQUIREMENTS

Education / Experience

Master in Chemistry

1-5 years in a Pharmaceutical Company.

Technical skills &

Competencies / Language

• Analytical ability
• Trouble shootings
• Co ordination
• Communication

Behavioural Competencies

(LEAD and others)

• Accountability, Authenticity, Collaboration, Courage and Trust