JOB DESCRIPTION:
- Having adequate knowledge of Sampling, Testing of Raw material, Packing Material, Finish Product, Validation and Stability samples.
- Sound knowledge of current industrial regulations and analytical method validation/verification activities.
- Having adequate knowledge of Laboratory Instruments and equipment’s Calibration, Maintenance/External calibration.
- Having adequate knowledge of Preparation of laboratory chemicals, Reagents, test solution, and Volumetric solution.
- Having adequate knowledge of Reference, Chemical and Working standard management i.e., Working Standard qualification and support in working standard management.
- Having adequate knowledge of Data entry in SAP.
- Having adequate knowledge of operation and trouble shoot of HPLC/UV/IR and other QC analytical instruments and its software. Having adequate knowledge of data entry management in inventory/Information management software of QC like LIMS software.
- Having adequate knowledge of preparation of the QC documents like SOPs, Protocols and general documentation.
- Having adequate knowledge of Pharma Industry Guidelines and Pharmacopoeias.
- Having exposure of regulatory audit and GDP/DI compliance.
- Having adequate knowledge of GLP / GMP requirements.
The base pay for this position is
N/A
In specific locations, the pay range may vary from the range posted.
JOB FAMILY:
Operations Quality
DIVISION:
EPD Established Pharma
LOCATION:
India > Village Mauza : Baddi
ADDITIONAL LOCATIONS:
WORK SHIFT:
Standard
TRAVEL:
Not specified
MEDICAL SURVEILLANCE:
Not Applicable
SIGNIFICANT WORK ACTIVITIES:
Continuous walking for prolonged periods (more than 2 hours at a time in an 8 hour day)