Posted:2 weeks ago|
Platform:
On-site
Part Time
Method Development of different drug product
Routine analysis of development samples and lab stability samples
GMP batch analysis, Stability batch analysis and reporting
Peer review for the routine experiment
PDLIMS data entry
Analysis of raw material and packaging material
Validation of analytical methods
Calibration and maintenance of analytical instruments
Preparation of tentative test procedures for routine development analysis, method
development, method validation report and standard test procedure
Follow GxP (GMP, GDP etc) for all processes
Following in-house compliance system
Maintain hygienic condition in respective department.
Ensure use of Personal Protective Equipment & attend EHS training & send waste to
concerned person & comply EHS requirements
Refrigerator temperature monitoring and maintenance.
Ensure data integrity
Piramal Pharma Solutions
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