5 - 10 years
0 Lacs
Posted:2 days ago|
Platform:
On-site
Full Time
Method Development: Develop and optimize analytical methods for drug products using techniques like HPLC, GC, GC-MS, and LC-MS.
Method Validation and Transfer: Execute and manage method validation, including creating protocols and reports, and oversee the transfer of these methods to other departments or sites.
Testing and Analysis: Perform quality control testing on raw materials, in-process samples, and finished products.
Instrumentation: Handle the calibration, preventive maintenance, and troubleshooting of laboratory instruments.
Data and Documentation: Maintain accurate records of all experimental data, write reports, and ensure compliance with cGMP and data integrity requirements.
Collaboration: Work with cross-functional teams, such as manufacturing, discovery, and quality assurance, to resolve issues and support product development.
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