Role & responsibilities
Perform routine and non-routine elemental analysis using ICPMS.
Prepare samples, standards, reagents, and calibration solutions as per approved SOPs.
Operate, calibrate, and maintain ICPMS/ AAS instruments.
Perform analysis of metals/elements such as Lead, Cadmium, Arsenic, Mercury, Copper, Iron, Zinc, Calcium, Magnesium, etc., as applicable in pharmaceutical products.
Follow approved test methods, SOPs, specifications, and pharmacopoeial/standard methods.
Conduct instrument suitability, calibration, system checks, and performance verification.
Record analytical observations and results accurately in worksheets, logbooks, and laboratory systems.
Ensure compliance with USFDA, GLP, GMP, NABL/ISO 17025 and internal quality requirements.
Investigate abnormal results, deviations, OOS/OOT results, and analytical discrepancies.
Maintain proper documentation and ensure data integrity.
Perform routine cleaning and preventive maintenance of instruments.




Coordinate with the QA/QC team regarding analytical results and documentation.
Ensure proper handling, storage, and disposal of samples and chemicals.
Participate in method verification/validation and laboratory quality-control activities.
Maintain laboratory safety and housekeeping standards.

Required Skills
Hands-on experience in ICPMS/ AAS operation and elemental analysis.
Valuable knowledge of sample digestion and preparation techniques.
Knowledge of calibration curves, standards, blanks, controls, and analytical calculations.
Understanding of GLP, GMP, NABL and ISO 17025 requirements.
Valuable documentation and reporting skills.
Ability to troubleshoot basic AAS-related issues.
Must have exposure of USFDA
Valuable knowledge of MS Excel and laboratory documentation

📌 Aas/icpms Analyst Usfda Lab Manesar
🏢 Arbro Pharmaceuticals
📍 Manesar