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Piramal Pharma

Trainee - Production

Turbhe,MH

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hirly's read of this role

Seniority
Entry level
Country
IN
Work mode
On-site / unstated
First seen by hirly
27 Sept 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

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Division

Piramal Pharma Solutions 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

Trainee - Production Job Description

  • We are looking for a Trainee – Production to support peptide manufacturing operations and gain hands-on experience in a GMP-regulated pharmaceutical environment. The role involves assisting in peptide synthesis, purification, documentation, equipment operation, and process improvement while ensuring compliance with safety and quality standards. This position offers an excellent opportunity for fresh graduates to develop technical skills and build a career in peptide manufacturing.
  • 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.
Original posting on Piramal Pharma's site ↗

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