QC Positions for B.Pharma/ M. Pharma @ Zydus Cadila | Attend the Walk-In Drive

No. of Posts:   1

Salary:   INR 3,00,000 – 7,00,000 P.A.

Job Description:  

• To maintain and adherence of the GLP and safety procedures in laboratory.
• To raise the request for issuance of work data sheet / protocols.
• To maintain instruments log books properly as per analysis.
• To acquire training from concerned person to update the cGMP system update technical knowledge.
• To perform the analysis as per work allocation and records the results in work sheet / protocol and maintain on line documentation.
• To work as Analyst / Operator as a level of users and maintain the CFR 21 part -11 compliance by following laid down procedures.
• To perform all the HPLC related analysis of In-process, intermediate, finished products & returned goods / raw materials Hold time / Stability study /reference / working standard analysis as per laid down specification & test procedures , SOPs, as per work allocation and report the analysis data in LIMS modules and report to Section Head / Or QC head.
• To ensure that every specification and method of analysis used of right product/material code.
• To follow the instruction of Shift /Section In charge for analysis /planning.
• To report any QI/NQI/OOS/OOT / Deviation/ discrepancy in laboratory analysis to QC- In charge.
• Responsible for performing calibration of laboratory instruments as per schedule and laid down SOPs with documentation and updation of instrument calibration status tag.
• To record and ensure all the entries, and results are in line with current specifications and STPs.
• To prepare standard operating procedures, work data sheets and other documents related to QC.
• To ensure the all column performance and column entry are maintain in column logbooks.
• To record analytical data in work data sheets / protocols for raw material / packing materials/intermediates /APIs and etc… As per current specification and method of analysis.
• Preparation, qualification and management of working standard for Raw materials Intermediates/APIs.
• To maintain reference / working standard/impurity standard usage records.
• Review of in-process analysis data and approval for further processing of the batch.
• To maintain instrument history record.
• Joint analysis with R&D personnel during analytical method transfer on HPLC.
• Preparation of stability protocols and stability reports.
• To perform analysis of stability samples as per stability schedule
• Daily monitoring and recording of temperature and humidity of refrigerator / working standard chamber and laboratory area.
• Perform holding time study of intermediates and preparation of reports.
• To prepare/ check the protocols & reports for analytical method validation and analytical method transfer
• Inform and Investigate OOS results in RM/Intermediates/APIs
• Initiation of change control / deviations / QI /NQI/ OOT related to QC.
• Ensure CFR 21 part -11 compliance and follow good chromatography practices during analysis, integration and reviewing of on line and off line chromatographic analysis to maintain proper data integrity.

Qualifications:  

• Experience range – 3 to 10 Years
• Education – B.Sc. /M.Sc. , B.Pharma/ M. Pharma

Application Instructions: 

• [email protected]

Walk-In Details  

• Date of Interview – 13.10.2017 (Friday)
• Time of Interview – 11.30 To 3.30
• Venue of Interview –  Cadila Pharmaceuticals Ltd. Plot No. 294, GIDC, Ankleshwar, Gujarat, India

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