Manager - TSD

Piramal Pharma Ltd; Kohir mandal; On-site; INR 1,500,000 - 2,500,000; Full time

Job summary

Piramal Pharma Solutions is seeking a Process Engineer / Technology Transfer Manager to drive technology transfer, scale-up, and commercial manufacturing of pharmaceutical products. You will oversee pilot plant campaigns, evaluate scale-up feasibility, and ensure robust process controls while maintaining cGMP compliance.

The role requires collaboration with R&D, Production, QA/QC, Engineering, EHS, and Supply Chain teams to deliver successful transfers and validated processes for commercial

Qualifications

• Strong process engineering knowledge and problem-solving skills.
• Experience with pilot plant campaigns and scale-up activities.
• Familiarity with cGMP, Batch Manufacturing Records, and change control.
• Ability to coordinate cross-functional teams.
• Strong root cause analysis and CAPA capabilities.

Responsibilities

• Execute technology transfer from R&D to pilot plant and manufacturing.
• Plan pilot plant campaigns, engineering batches, trial batches, and validations.
• Review PFDs, P&IDs and process mapping documents.
• Perform HAZOP studies and risk assessments.
• Support CAPA investigations and change control.
• Coordinate with R&D, Production, QA, QC, EHS, and Supply Chain.
• Ensure compliance with cGMP and regulatory requirements.
• Support process validation and equipment qualification.
• Drive continuous improvement and cost optimization.

Skills

Process engineering

Technology transfer

Cross-functional collaboration

Education

Bachelor of Technology (BTech)

Job description

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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

Manager - TSD

Job Description

We are seeking a Process Engineer / Technology Transfer Manager to support technology transfer, process scale-up, and commercial manufacturing of pharmaceutical/API products. The role involves executing pilot plant, validation, and commercial batches, optimizing manufacturing processes, providing technical support for production, review engineering documentation, participating in HAZOP and process risk assessments, and ensuring compliance with cGMP requirements. The ideal candidate should possess strong process engineering knowledge, problem-solving skills, and the ability to collaborate effectively with cross-functional teams to successfully transfer and commercialize manufacturing processes.

Process Engineer / Technology Transfer Manager

Key Responsibilities:

• Execute technology transfer activities from R&D to pilot plant and commercial manufacturing.
• Evaluate process feasibility for scale-up.
• Plan and execute pilot plant campaigns, engineering batches, trial batches, and process validation batches.
• Perform process scale-up activities while ensuring product quality, process safety, and regulatory compliance.
• Provide technical support for troubleshooting and process optimization.
• Review Process Flow Diagrams (PFDs), Piping & Instrumentation Diagrams (P&IDs), and process mapping documents.
• Conduct HAZOP studies and participate in process risk assessments to identify and mitigate operational hazards.
• Evaluate process performance, identify bottlenecks, and implement continuous improvement initiatives.
• Review GMP-compliant documentation, including Batch Manufacturing Records (BMRs), SOPs, and technology transfer documents.
• Investigate manufacturing deviations, perform root cause analysis, and prepare investigation reports with appropriate CAPA recommendations.
• Manage Engineering Change Requests (ECRs) and support change control implementation.
• Coordinate with R&D, Production, Quality Assurance, Quality Control, Engineering, EHS, and Supply Chain teams to ensure successful project execution.
• Ensure compliance with cGMP, quality systems, process safety, and regulatory requirements throughout the product lifecycle.
• Support process validation, equipment qualification, and commercial manufacturing activities.

Participate in continuous process improvement, cost optimization, and manufacturing efficiency enhancement initiatives

Bachelor of Technology (BTech)