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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

Job Description

Brief Job Summary: -

            Carrying out of Production operations in compliance to cGMP & EHS requirements.

 Responsibilities: -

• Planning and ensuring of raw material availability for daily production as per production plan.

• Operation and cleaning of process equipment’s Viz. Reactor, centrifuge, Tray drier, Vacuum Tray drier/ Roto cone vacuum drier/ Agitated Nutsche filter cum drier/ Distillation column/ filters, miller & sifter operations etc., utility equipment’s viz. vacuum pump, Ejectors, scrubbers etc. allocated.
• Adherence to cGMP (current Good Manufacturing Practice), GDP (Good documentation practice) and EHS requirements.
• Monitoring & controlling the process parameters as per BMR without any deviation.
• Execution of production plan and meeting the production targets.
• Effective utilization of men, utility, equipment, raw materials, and power.
• Issue and Control of Intermediates.
• Maintaining Good Housekeeping in workplace and shopfloor.
• Online Documentation viz. batch manufacturing record, cleaning record etc without any data integrity.
• Trouble shooting of process equipment’s, utility systems and process.
• Initiating work order and safety permits as per procedure.
• Generating new ideas and initiatives
• Involving Yield improvement, time cycle reduction, capacity enhancement initiatives.
• Making the plant for the audit readiness.
• Ensuring the safety of self, operating personnel, workmen and machine associated and knowledge on static electricity and its control.
• Coordination with the supporting departments for smooth running of production.
• Participation in training program and effective communication process.
• Reporting of near miss, unsafe act and unsafe condition.
• Handling of Hazardous operation and chemicals in safe manner.
• Proper communication and spot relieving during shift change over in the shop floor.
• Sampling and submission of in-process samples and receiving the results from QC/ ARD.

Qualification:

B.Sc (Chemistry) / Diploma in Chemical

Experience: 3-6 Years experience in Pharma Production activities