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.

- Good 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.

- Good 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 Private
📍 Manesar