Job Description

Perform analysis of raw materials, intermediates, in-process samples, solvents, recovered solvents, and finished APIs as per approved specifications and analytical methods.

Carry Out Testing Using Techniques Such As

HPLC

GC

UV-Visible Spectrophotometer

FTIR

KF / moisture determination

pH

Titration

Melting point

Specific gravity and other applicable physical/chemical tests.

Perform testing of solvent recovery samples for purity and relevant quality parameters.

Ensure testing is performed within defined timelines.

  • Instrument Handling

Operate analytical instruments as per approved SOPs.

Perform routine instrument checks and ensure instruments are in calibrated/qualified status before use.

Maintain instrument logbooks and usage records.

Report instrument malfunction, abnormal results, or breakdowns to the supervisor.

Assist in instrument calibration, qualification, and troubleshooting activities.

  • Documentation & Data Integrity

Record analytical results accurately in worksheets, laboratory notebooks, LIMS, COA, and other approved formats, as applicable.

Follow Good Documentation Practices (GDP) and data integrity principles.

Ensure all raw data, chromatograms, calculations, observations, and results are complete and traceable.

Review analytical calculations and documentation before submission.

Maintain proper records of standards, reagents, solutions, and reference materials.

  • OOS / OOT & Investigation

Immediately report Out-of-Specification (OOS), Out-of-Trend (OOT), atypical, or abnormal results.

Support laboratory investigations and root-cause analysis.

Participate in OOS/OOT investigations as per approved procedures.

Ensure investigation activities and supporting analytical data are properly documented.

  • Reagents, Standards & Laboratory Management

Prepare and standardize reagents, volumetric solutions, mobile phases, buffers, and other laboratory solutions as per approved procedures.

Maintain proper labeling, storage, and expiry/retest information for reagents and solutions.

Maintain reference standards and working standards as per applicable procedures.

Monitor laboratory consumables and inform the supervisor regarding shortages.

  • Stability & Validation Support

Perform testing of stability samples according to approved stability protocols.

Support method validation, method verification, analytical method transfer, and cleaning validation activities as required.

Generate and maintain analytical data and supporting documentation.

  • GMP & Safety Compliance

Follow applicable GMP, GLP, SOP, EHS, and laboratory safety requirements.

Handle chemicals, solvents, acids, bases, and hazardous materials using appropriate PPE and safety procedures.


Job Details

Role Level: Not Applicable Work Type: Full-Time
Country: India City: Mumbai
Company Website: https://www.cadilapharma.com/ Job Function: General Management
Company Industry/
Sector:
Pharmaceutical Manufacturing

What We Offer


About the Company

Searching, interviewing and hiring are all part of the professional life. The TALENTMATE Portal idea is to fill and help professionals doing one of them by bringing together the requisites under One Roof. Whether you're hunting for your Next Job Opportunity or Looking for Potential Employers, we're here to lend you a Helping Hand.

Report

Disclaimer: talentmate.com is only a platform to bring jobseekers & employers together. Applicants are advised to research the bonafides of the prospective employer independently. We do NOT endorse any requests for money payments and strictly advice against sharing personal or bank related information. We also recommend you visit Security Advice for more information. If you suspect any fraud or malpractice, email us at abuse@talentmate.com.


Recent Jobs
View More Jobs
Talentmate Instagram Talentmate Facebook Talentmate YouTube Talentmate LinkedIn