Work as Respi CoE Analyst at Cipla

Cipla, as an organisation has been built brick-by-brick on the foundation of care. Caring For Life has always been and continues to remain, our guiding purpose. Driven by the same purpose, we have extended our presence to 80+ countries providing over 1,500 products across various therapeutic categories in 50+ dosage forms. To make healthcare more affordable globally, we are deepening our presence in the key markets of India, South Africa, the U.S. among other economies of the emerging world.

Post : Respi CoE Analyst

Job Description
Accountability Cluster
I. Develop new analytical methods for analysis of routine as well as stability samples by following proper GLPs to provide results or information regarding products to formulators
II. Perform maintenance and calibration of lab instruments / equipment to get accurate and reproducible analytical result for proper interpretation
III. Document and interpret the analytical data in a timely manner as per GLP / GMP requirements to maintain records and compliance of regulatory norms
IV. Provide support to units or CFTs for transfer of analytical methods and techniques by visiting and demonstrating them with the relevant analysis to ensure successful and timely transfer of products
V. Maintain proper safety, GLP, and GMP environment in the work place to minimize accidents and incidents
VI. Review the analytical requirements and recommend corrections in specifications by coordinating with units and CFTs to ensure smooth operations

Major Activities / Tasks
• Perform part method validation, forced degradation studies, excipient compatibility studies, reverse engineering, add-mixture studies, in-use studies, hold-time study and analysis of routine & stability studies
• Conduct cleaning validation studies
• Perform analysis of API, excipients and secondary material (packaging material, ink, adhesive etc.)
• Develop cost effective & time saving analytical method for new or existing product
• Evaluate the pharmacopeia and verify the documents
• Maintain the lab instruments / equipment and troubleshoot the issues
• Perform calibration (schedule / breakdown) and calculate instrument utilisation
• Up-keep the HPLC/GC/IC columns as per cGLP
• Record and document all analytical activities in timely manner in Lab note-book, instrument/equipment and column log book
• Provide base documents for MOA / COA preparation for better coordination in analytical studies
• Transfer methods and technologies to other units and departments
• Study the literature to resolve units and regulatory queries and conduct investigation studies in stipulated time period
• Analyse samples at pilot plant and unit for trace determination (Cleaning Validation)
• Follow safety guidelines by ensuring use of PPE & MSDS of chemicals at time of analysis
• Upkeep the samples given for analysis and ensure timely destruction after analysis as per SOP
• Dispose solvents and waste generated during the analysis
• Arrange analytical requirements like column, impurities, standards, placebo and samples for units and other department like Validation Lab or Outsourced Lab
• Review and recommend corrections in the MOA, COA & Specifications

Candidate Profile
• M. Sc. (Analytical Chemistry) / M. Pharm.
• 2-4 years of experience in pharmaceutical organisation with knowledge of handling instruments like HPLC, GC, Dissolution tester and DPI related instruments
• Knowledge of current guidelines like ICH, EMEA, WHO

Additional Information
Experience : 2-4 years
Qualification : Graduate in Pharmacy or Life Sciences
Location : Mumbai
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : LCM
End Date : 30th October 2025