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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

• Development and execution of NCE projects, generic projects and line extension projects using QbD principle.
• Preparation of literature summary and development report to the assigned product.
• Involve in execution of formulation development, process development and manufacturing of GMP batches to the assigned product.
• Preparation of technical documents like MFC, BMR, BPR and Stability protocol etc. following the GDP.
• Follow GxP (GMP, GDP etc.) for all processes and train the subordinates to follow the same.
• Execution of scale up and pilot/clinical batches in pilot under GMP condition.
• Performing calibration and maintenance of R&D instruments and equipment
• Procuring/ indenting materials and machines change parts related to concern projects
• Maintain safe and hygienic condition in respective department
• Ensuring the use of personal protective equipment whenever required during batch execution
• Attending training related to FD, EHS and QA (as applicable)
• All generated waste to be sent to concerned person and must be comply with EHS requirements
• Preparation of technical presentations and presenting to client