Apprentice

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Division

Piramal Pharma Solutions

Piramal Pharma Solutions is a contract development and manufacturing  organization (CDMO), offering end-to-end development and manufacturing  solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia.  

This enables us to offer a comprehensive range of services including Drug Discovery  Solutions, Process & Pharmaceutical Development services, Clinical Trial  Supplies, Commercial supply of APIs and Finished dosage forms. We also offer  specialized services like development and manufacture of Highly Potent APIs  and Antibody Drug Conjugation.  

Our capability as an integrated service provider  & experience with various technologies enables us to serve Innovator and  Generic companies worldwide.  

For more details, please visit : www.piramalpharmasolutions.com

Job Title

Apprentice

Job Description

JD - Apprentice QC

To execute sampling and analysis of Raw materials along with relevant laboratory documentation.

To execute analysis of finished goods, In-process, packing materials and cleaning samples along with relevant laboratory documentation.

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.

To execute Analytical Method Validation / Transfer, cleaning validation as per approved procedure & protocol.

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.