ADL (Officer/Sr.Officer/Executive )
2 months ago
We are seeking a highly skilled person to join the team in the pharmaceutical industry. The ideal candidate will be responsible for method development and validation, as well as routine and stability analysis utilizing a variety of analytical techniques including High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), Dissolution testing, and Karl Fischer titration.
- Develop and validate analytical methods for the quantitative analysis of pharmaceutical compounds using HPLC, GC, Dissolution, and KF techniques.
- Perform routine analysis of pharmaceutical samples according to established protocols and procedures.
- Conduct stability studies to assess the stability of pharmaceutical formulations over time.
- Troubleshoot and optimize analytical methods to ensure accuracy, precision, and reliability of results.
- Maintain accurate records of all analyses, method development, and validation activities in compliance with regulatory guidelines.
- Collaborate with cross-functional teams including R&D, Quality Control, and Regulatory Affairs to support product development and regulatory submissions.
- Stay current with developments in analytical techniques, instrumentation, and regulatory requirements in the pharmaceutical industry.
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