Sr. Principal Scientist - Analytical

Business: Piramal Critical Care
Department: Research and Development
Location: Rabale, Navi Mumbai
Travel: Low:

Head Process development & technology

Reporting to this role will be Research Associates

• Lead and Perform the analytical method development and validation for APIs, specialty chemicals, and raw materials using techniques like HPLC, GC etc
• Independently execute experimental plans, interpret data, and propose solutions to technical challenges in collaboration with managers.
• Support routine analysis and ensure the generation, interpretation, and review of experimental data to meet project timelines.
• Apply advanced analytical chemistry techniques to develop robust testing methods for new products.

• Provide on-site or remote support for analytical method transfer, including document review, gap analysis, and coordination between sending and receiving sites.
• Prepare and review analytical method transfer documents (e. g. , assessment reports, transfer plans, protocols, and stability data).
• Collaborate with internal and external stakeholders to resolve queries and ensure smooth transfer execution.
• Business and Plant Support
• Troubleshoot and resolve research and analytical issues promptly.

• Maintain and manage research data, ensure adherence to documentation standards, and implement SOPs in the R&D lab.
• Oversee lab operations, including reagent and column inventory management, instrument calibration, and IQ/OQ/PQ documentation.
• Coordinate lab housekeeping and renewal of annual maintenance contracts for analytical instruments.

• Supervise and mentor team members, ensuring adherence to safety protocols and fostering competency development within the team

Key Competencies:

• Strong expertise in analytical chemistry and industrial experience with analytical techniques.
• Proficient in operating instruments like HPLC, GC, GC-HS, GCMS and LCMS, with experience in data analysis and interpretation (HPLC, GC, NMR, mass spectra)
• Skilled in analytical method development, validation, and transfer in compliance with ICH guidelines, GLP, and GMP standards.
• Well versed with ICH, WHO and various guidelines.
• Handled plant, regulatory, and QA-related analytical queries, including impurity standards, method improvements, and development.
• Familiarity with plant operations, quality systems, and troubleshooting analytical challenges.
• E & L experience will be an added advantage.

• Ability to interpret complex data, draw actionable conclusions, and effectively communicate results.
• Proficient in technical writing, including preparation of analytical documents and reports.

Digital and Technical Tools

• Competent in MS Office applications (Word, Excel, PowerPoint) and internet-based research tools
• Knowledge of SAP and sourcing tools for effective workflow and resource management.