Apprentice

12 hours ago

Mahad, India Piramal Pharma Solutions Full time

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.
- 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, 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.
- Destruction of QC Samples like Retention samples, analyzed samples etc.
- 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.
- 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.
- Ensuring good housekeeping 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 ensure disposal of waste.

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