Job Overview
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Date PostedApril 5, 2024
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Location (State / UT)
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Expiration dateApril 15, 2026
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Experience2 Years, 4 Years
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GenderAny
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Desired QualificationMaster’s Degree
Job Description
Execute the core method development activities and conduct analysis of routine as well as stability samples to finalize specifications and ensure timely delivery of the product to the unit.
Key Accountabilities
- Develop new analytical methods for the analysis of routine as well as stability samples by following proper GLPs to provide results or information regarding products to formulators
- Perform maintenance and calibration of lab instruments/equipment to get accurate and reproducible analytical results for proper interpretation
- Document and interpret the analytical data in a timely manner as per GLP / GMP requirements to maintain records and compliance of regulatory norms
- 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
- Maintain proper safety, GLP, and GMP environment in the workplace to minimize accidents and incidents
- Review the analytical requirements and recommend corrections in specifications by coordinating with units and CFTs to ensure smooth operations
Education Qualification
M. Sc. (Analytical Chemistry) / M. Pharm
Relevant Work Experience
- 2-4 years of experience in a pharmaceutical organization with knowledge of handling instruments like HPLC, GC, Dissolution tester, and DPI-related instruments
- Knowledge of current guidelines like ICH, EMEA, WHO
Division
Integrated Product Development
Department
Global Respiratory
Sub Department 1
Respiratory -Formulations R&D – DPI