Role: Executive / Senior Executive - LCMS
Location: Mahad, Maharashtra
Department: ADL (API)
Notice Period: 15 Days/1 Month
Key Responsibilities
- Instrument Handling: Operate and maintain LCMS instruments for qualitative and quantitative analysis; Troubleshoot and calibrate LCMS instruments to ensure optimal performance.
- Sample Preparation: Perform sample preparation techniques like extraction, dilution, and purification for analysis; Ensure proper handling and documentation of samples.
- Analytical Method Development: Develop and validate LCMS methods as per regulatory guidelines; Optimize parameters to improve sensitivity, accuracy, and efficiency.
- Data Analysis and Reporting: Analyze LCMS data using specialized software and prepare detailed reports; Interpret mass spectra to identify compounds and assess sample purity.
- Compliance and Documentation: Maintain accurate records as per Good Laboratory Practices (GLP) or Good Manufacturing Practices (GMP); Ensure compliance with regulatory and safety standards (e.g., ICH, FDA, ISO).
- Collaboration: Work closely with R&D, QA, and other teams to support projects; Train and mentor team members on LCMS techniques.
Qualifications
Educational Background:
Experience: 2–6 years of experience in LCMS operation and method development.
Skills:
Proficiency in LCMS software (e.g., Thermo Fisher Scientific, Chromeleon HPLC).
Strong analytical and problem-solving abilities.
Knowledge of regulatory guidelines (e.g., USFDA, EMA).
Preferred Experience
Handling bioanalytical or pharmaceutical samples.
Experience in impurity Nitrosoamine, NDSRI, and Genotoxic impurities.
Familiarity with related techniques like HPLC, LCMS.
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