Greetings from the Apnar Pharma !!!
We have a requirement in Quality Control Department - Formulation.
Job Description:
- Responsible to perform routine activity as per current GDP, GMP
- A sampling of raw material and Packing material.
- Preparation of STP, TDS and SOPs related to Quality control laboratory.
- Able to handle all sophisticated Instruments of the QC Dept along with troubleshooting on a routine basis ( Like HPLC/GC/UV/KF /Autotitrator / Dissolution etc.)
- Analysis of Raw Material, packing material, In-process samples, Finished product and stability samples.
- Calibration and verification of analytical Instruments and equipment used in Quality control Laboratory.
- Preparation of Method Verification protocol & Report in concern of In-house method as well as for compendial methods.
- Performing Method verification for different products.
- Working standard Qualification.
- Responsible for Preparation of reagent Volumetric solution & standardization of Volumetric solution
- Maintenance of usage records for Working/Reference standards, impurity standards and HPLC/GC columns.
- Performing Excel sheet Validation/Verification as per requirement.
- Responsible for handling Column Management.
- Able to perform online reporting with analysis activity,
- As per Management requirements, the Head of the department can allocate additional Job Responsibility
If you know suitable candidates, please inform them to forward their updated Resume on hr@apnarpharma.in
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