About the role

Key Responsibilities:

We are looking for an experienced and strong expertise in LC-MS/MS and GC-MS/MS to join us.

Develop and validate analytical methods for LC-MS/MS and GC-MS/MS systems.
Troubleshoot instrument and method-related issues on Agilent, Waters, and AB Sciex platforms.
Ensure compliance with regulatory guidelines (ICH, FDA, EMA) for impurity profiling.
Prepare and review validation protocols, reports, and SOPs.
Required Skills & Experience:
Hands-on experience with LC-MS/MS and GC-MS/MS instrumentation (Agilent, Waters, AB Sciex).
Strong knowledge of GTI and Nitrosamine analysis in pharmaceutical matrices.
Expertise in method development, optimization, and troubleshooting.
Familiarity with regulatory requirements for impurity testing.
Minimum 5-6 years of experience in pharmaceutical

Preferred Qualifications:

Expertise in LC-MS/MS and GC-MS/MS