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
- Master's in Analytical Chemistry, Pharmaceutical Sciences,
- Experience with software like MassHunter, Analyst, Empower, etc.
Skills: lc-ms/ms and gc-ms/ms,strong knowledge of gti and nitrosamine,instrumentation
