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)