Chief Principal Scientist – Technology Transfer
Location: Rabale, Maharashtra
Department: Business Development / R&D
Company: Piramal Critical Care
Employment Type: Full-Time
Experience Required: 12–15 Years
Qualification: M.Pharm
Salary Range (Estimated)
₹28 – ₹45 LPA CTC
Depending on experience in sterile injectables, technology transfer, formulation development, and leadership responsibilities.
Job Overview
Piramal Critical Care is seeking an experienced Chief Principal Scientist – Technology Transfer to lead pharmaceutical development, scale-up, and technology transfer activities for sterile injectable products. The role requires expertise in formulation development, process optimization, technology transfer, regulatory compliance, and project management while working closely with internal teams, CMOs, CROs, and global stakeholders.
Key Responsibilities
Technology Transfer
Lead end-to-end technology transfer and scale-up activities for sterile injectable products.
Execute successful transfer of products from R&D to commercial manufacturing sites.
Coordinate technology transfer activities with internal manufacturing sites and external CMOs/CROs.
Prepare and review Technology Transfer Documents (TTD), protocols, reports, and manufacturing documents.
Support process validation and commercial batch execution activities.
Formulation Development
Design and execute formulation development activities for injectable products.
Conduct pre-formulation studies, formulation optimization, and process troubleshooting.
Apply Quality by Design (QbD) principles and risk assessment methodologies.
Develop robust and scalable manufacturing processes.
Project Management
Plan, execute, and monitor development projects from concept to commercialization.
Prepare project budgets, timelines, and resource plans.
Track project milestones and ensure timely delivery.
Evaluate technical feasibility of new product opportunities.
Cross-Functional Collaboration
Collaborate with Regulatory Affairs, QA, QC, Microbiology, Manufacturing, Supply Chain, and Business Development teams.
Support customer audits, technical discussions, and product evaluations.
Provide technical expertise during customer and regulatory interactions.
Compliance & Documentation
Ensure compliance with GMP, GLP, ICH Guidelines, and EHS requirements.
Review and approve BMRs, BPRs, MFRs, MPRs, SOPs, and Product Development Reports.
Maintain accurate development documentation and laboratory records.
Support audit readiness and regulatory inspections.
Leadership & Team Development
Mentor and guide formulation scientists and project team members.
Conduct technical training and capability development programs.
Support laboratory infrastructure, equipment qualification, and continuous improvement initiatives.
Required Qualifications
Master’s Degree in Pharmacy (M.Pharm).
12–15 years of industrial experience in pharmaceutical development and technology transfer.
Strong experience in Sterile Injectable Product Development.
Experience handling technology transfer projects across manufacturing sites and CMOs.
Knowledge of formulation development for US, Europe, Japan, and regulated markets.
Uttar Pradesh :
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