Conduct analytical testing of samples under supervision using instruments such as
HPLC, GC, LC-MS/MS, and UV Spectrophotometer
.
Prepare
reagents, solutions, and standards
in accordance with approved
Standard Operating Procedures (SOPs)
.
Record and maintain
raw data, analytical logs, and reports
accurately as per
GLP/GMP
requirements.
Ensure all documentation meets
regulatory, quality, and internal audit
compliance standards.
Support
analytical method development and validation
activities for pharmaceutical and biologic products.
Assist in routine calibration, instrument upkeep, and troubleshooting under guidance.
Participate actively in
training programs
to enhance technical skills and understanding of analytical techniques.
Follow laboratory safety procedures and maintain a compliant, organized work area.
Experience Required:
2-3 years
of hands-on experience in an analytical laboratory environment.
Working knowledge of
GLP, GMP
, and related quality systems (preferred).
* Exposure to analytical instrumentation such as HPLC, GC, LC-MS/MS, UV, etc.
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