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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

• Verify the availability and readiness of required resources such as raw materials and clean apparatus/equipment prior to production. Plan and execute production activities in compliance with cGMP and GDP guidelines.
• Oversee labelling activities, BMR/ECR documentation, line clearance procedures, and area cleaning processes.
• Review and authorize work orders as required. Supervise in-process sampling, final material sampling, and packing activities.
• Report equipment breakdowns, deviations, or abnormal observations to departmental seniors promptly.
• Read, review, and ensure adherence to all relevant SOPs. Review BMR, ECR, and all other production-related documentation for accuracy and compliance.
• Supervise equipment verification, calibration, and qualification activities, and ensure preventive maintenance of critical instruments and equipment is completed.
• Oversee cleaning activities for equipment, instruments, and apparatus to maintain compliance. In the absence of the assigned employee, the designated deputy will assume responsibility for the above duties.
• Supervise dispatch-related activities to ensure proper handling and documentation. Promote and maintain safety awareness and compliance within the production area.
• Ensure timely updates and reporting of in-process batch status and results. Maintain and support production quality through proper management of change controls, deviations, CAPA, OOS, OOT, and customer commitments.
• Collaborate with cross-functional departments to plan and allocate resources effectively, ensuring smooth production execution and optimal utilization of internal and external resources.