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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

• Understand and follow standard operating procedures (SOPs) for peptide synthesis & Purification.
• Assist in the preparation of reagents, solutions, and equipment for peptide production.
• Execute peptide synthesis/purification under the guidance of experienced personnel
• Learn and perform purification techniques such as HPLC, chromatography, and filtration.
• Assist in maintaining accurate records of production and testing activities.
• Follow Good Manufacturing Practices (GMP) and safety guidelines.
• Learn to operate and maintain peptide production equipment.
• Report equipment malfunctions or abnormalities promptly.
• Maintain accurate and detailed records of all production activities.
• Compile data and assist in preparing production reports.
• Communicate effectively with team members and supervisors.
• Contribute to the identification and implementation of process improvements.
• Provide feedback on procedures to enhance efficiency and quality
• Attend training sessions to enhance knowledge and skills.
• Actively participate in professional development opportunities.