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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

• Adhere to Piramal core values, PSF, safety guidelines, quality standards, SOPs, and cGMP requirements.
• Complete all assigned mandatory, technical, and functional trainings within the defined timelines.
• Execute planned experiments related to peptide synthesis and purification as per approved procedures and experimental plans.
• Maintain accurate, complete, and timely records of all experimental activities, observations, and results.
• Ensure timely online documentation and data entry in accordance with data integrity and documentation requirements.
• Complete assigned projects, experiments, and work-related tasks within agreed timelines.
• Monitor project progress and proactively communicate any challenges, deviations, or delays.
• Support troubleshooting and process optimization activities related to peptide synthesis and purification.
• Collaborate with team members and provide technical or operational support whenever required.
• Share relevant experimental observations, technical knowledge, and learnings with team members.
• Monitor process parameters and variations observed during peptide purification and process development.
• Analyze process variations, identify trends or potential issues, and support appropriate corrective or optimization actions.
• Contribute to continuous improvement of peptide purification processes with a focus on consistency, efficiency, safety, and quality.
• Ensure all assigned activities are performed in accordance with applicable safety, quality, compliance, and organizational requirements.