Analyst - LC-MS/MS

Sipra Labs; Hyderabad; On-site; INR 600,000 - 900,000; Full time

Job summary

Sipra Labs Limited, a 30+ year US FDA-approved CRO serving Pharma, Biotech and Medical Device clients, seeks an Analyst - LC-MS/MS for its Analytical Lab in Hyderabad. The role covers assay, related substances, impurity profiling and elemental/extractable support on LC-MS/MS platforms (Waters/Sciex/Agilent), method execution, calibration and system-suitability checks, and SLIMS-based reporting.

The analyst will maintain raw data and logbooks per ALCOA+, support method validation/transfer, and

Qualifications

• MSc Analytical Chemistry or equivalent with 3-5 years hands-on LC-MS/MS experience in a regulated CRO or pharma QC laboratory.

Responsibilities

• Analyze assay, related substances, impurity profiling and elemental/extractable support on LC-MS/MS platforms.
• Perform method execution, calibration and system-suitability checks, and SLIMS-based reporting.
• Maintain raw data and logbooks per ALCOA+ and support method validation/transfer.
• Ensure compliance with cGMP, NABL 17025 and US FDA 21 CFR 211 requirements.

Skills

LC-MS/MS

ALCOA+

cGMP

GLP

Data integrity

Education

MSc Analytical Chemistry

Tools

Waters LC-MS/MS

Sciex LC-MS/MS

Agilent LC-MS/MS

Job description

Role & responsibilities:

Sipra Labs Limited, a 30+ year US FDA-approved Contract Research Organization serving Pharma, Biotech and Medical Device clients, seeks an Analyst - LC-MS/MS for its Analytical Lab in Hyderabad. The role covers assay, related substances, impurity profiling and elemental/extractable support on LC-MS/MS platforms (Waters/Sciex/Agilent), method execution, calibration and system-suitability checks, and SLIMS-based reporting. The analyst will maintain raw data and logbooks per ALCOA+, support method validation/transfer, and comply with cGMP, NABL 17025 and US FDA 21 CFR 211 requirements.

Preferred candidate profile:

M.Sc. (Analytical / Organic Chemistry) or equivalent, with 3-5 years hands-on LC-MS/MS experience in a regulated CRO or pharma QC laboratory.

Compliance requirement:

This position requires strict adherence to cGMP/GLP, 21 CFR Part 11 and data integrity (ALCOA+) principles, consistent with Sipra Labs status as a US FDA-approved and NABL (ISO/IEC 17025) accredited facility. Candidates with any prior data-integrity violation at a regulated employer will not be considered.