Job Description

KEY ACCOUNTABILITIES
Testing
Performing timely sampling and 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.
Good Laboratory Practice
Performing calibration & maintenance of lab. Equipment and assisting for the qualification of laboratory equipment.
Managing reference standards, working standards, laboratory reagents & chemicals.
Arranging and observing Control Samples and maintaining record.
Participating in Investigation of out of specification results, performing retesting.
Maintaining laboratory raw data related to testing activity.
Validation
Performing the validation exercise as per the protocol. Maintaining raw data related to validation.
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.
REQUIREMENTS
Education / Experience
Post Graduate in Science (Organic or Analytical Chemistry )
0-3 years in chemical & instrumental testing laboratory with exposure to GMP, GLP.
Technical skills &
Competencies / Language• Analytical ability
• Trouble shootings
• Co ordination
• Communication


Behavioral Competencies
(LEAD and others)• Accountability, Authenticity, Collaboration, Courage and Trust