Quality Control Assistant

Piramal Pharma


Not disclosed

Work from Office

Full Time

Min. 1 Years

Job Details

Job Description

Executive - Quality Control

Job Description:

  • To execute analysis of finished goods / Stability samples / Raw materials / Packing materials In-process and cleaning samples along with relevant laboratory documentation.
  • Intimation & result reporting after completion of analysis & relevant documentation.
  • Before starting an analysis, following points (but not limited to) must be checked:
  • Check all the instruments on the equipment required for the analysis are in working condition and are in calibrated state.
  • Checking and ensuring proper status labels after confirming availability of all the requirements (as applicable) for analysis such as approved control procedure, analytical protocol, reference standards, chemicals, reagents, GC/HPLC Columns, glassware, water preparation equipment, water bath, sonication baths, mobile phase bottle etc.
  • Ensure the online documents pertaining to day-to-day analysis are efficiently completed in timely manner. Reporting the activities daily to immediate supervisor.
  • Ensure timely calibration & preventive maintenance of equipment/instrument.
  • Destruction of respective records & QC samples like retention samples of raw materials, analyzed samples.
  • To take out the quality reports, data / results entry in SAP system.
  • To prepare and maintain the working standards & documentation.
  • Ensure timely raising and closure of deviations, quality events, change controls, OOS/OOT.
  • Execution of analytical method validation, cleaning validation of products.
  • Preparation and maintenance of Analytical data sheets and Excel spread sheets.
  • Adequate knowledge of all equipment/instruments & their functioning in the laboratory & assist in equipment/instrument qualification activities.
  • Ensuring the quality and integrity of all GxP data and documentation generated.
  • Ensuring effective execution requirements of food regulations (US)-21 CFR Part 111.
  • Ensure fully Engagement and Involvement regarding awareness, clarity maintained related to data integrity.
  • Ensure the 21 CFR Part 11 compliance in the laboratory.
  • Effective implementation of practices like cGMP & GLP, ISO 9001, ISO 14001, ISO 22000,  ISO 18001, HACCP and SQF in QC Dept.
  • To follow and maintain the standard chromatographic practices.
  • Ensuring good house-keeping and accident free working in the laboratory.
  • To perform safe Laboratory operations (as per MSDS) ensuring proper usage of PPEs, safe, secure storage of hazardous, toxic, explosive, corrosive, irritant materials.
  • Ensure proper maintenance of HPLC and GC column and related logbooks in QC lab.
  • To fulfill the analytical requirements of FSSAI regulation.
  • To undergo assigned trainings on cGMP, HSE & departmental procedures / policies. 
  • To determine internal and external QEHS issues as well as needs and expectations of relevant interested parties and monitor the same.
  • To implement QEHS policy & objectives.
  • To ensure participation and consultation of worker.
  • To identify & communicate incidents, QEHS non conformities, investigate and take corrective actions on the same.
  • To ensure work permit system during maintenance activities.
  • To implement QEHS continual improvement projects at site and monitor.

Job role

Work location

Mahad, Mahad, Piramal Enterprises Limited, Plot no. K-1, Additional M.I.D.C., Mahad, Maharashtra, India


Quality Assurance

Role / Category

Operations Quality Control

Employment type

Full Time


Day Shift

Job requirements


Min. 1 year

About company


Piramal Pharma

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