Research Analyst

Genotek Biochem

Hadapsar

On-site

INR 450,000 - 650,000

Full time

13 days ago
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Job summary

Genotek Biochem in Hadapsar (Pune) is seeking a Research Analyst with 2–5 years of hands-on experience in analytical testing, method development/validation, and routine analysis of raw materials, intermediates, and finished products in compliance with GLP/GMP.

You will operate HPLC, GC, UV-Vis, FTIR, and dissolution equipment, maintain records, support method transfer, investigations, CAPA, and contribute to SOP reviews while ensuring safety and regulatory compliance.

Qualifications

  • Must have strong knowledge of analytical chemistry and pharmaceutical/chemical analysis.
  • Hands-on experience with HPLC and other analytical instruments.
  • Understanding of method validation parameters (accuracy, precision, specificity, linearity, range, robustness, LOD, LOQ).
  • Familiarity with GMP/GLP and data integrity.
  • Ability to document chromatograms and test results accurately.

Responsibilities

  • Perform analytical testing of raw materials, intermediates, finished products, and stability samples.
  • Operate HPLC, GC, UV-Visible, FTIR, dissolution, pH, moisture/LOD.
  • Support analytical method development, optimization, and method transfer.
  • Perform analytical method validation/verification as per guidelines.
  • Prepare and maintain analytical solutions, reagents, mobile phases, standards, and reference materials.
  • Operate analytical instruments and ensure proper instrument usage, calibration, and maintenance.
  • Review analytical results and ensure accurate documentation of observations, calculations, chromatograms, and test results.
  • Investigate OOS/OOT results and support laboratory investigations and CAPA activities.
  • Maintain laboratory records, worksheets, logbooks, and analytical reports in GLP/GMP and SOP.
  • Coordinate with QA, QC, Production, R&D for analytical requirements.
  • Support preparation and review of analytical protocols, reports, specifications, and SOPs.
  • Ensure proper handling, labeling, storage, and disposal of samples and chemicals.
  • Maintain laboratory housekeeping and comply with EHS and safety requirements.
  • Participate in internal/external audits and provide required analytical documentation.
  • Stay updated with current analytical techniques and regulatory requirements.

Skills

Analytical chemistry
HPLC
Instrument operation
Data interpretation
GMP/GLP

Education

M.Sc./B.Sc. in Chemistry/Analytical Chemistry

Job description

Job Description Research Analyst
Department: ADL (Analytical Development Laboratory)
Designation: Research Analyst
Location: Hadpsar, Pune
Experience: 2-5 Years
Qualification: M.Sc./B.Sc. in Chemistry / Analytical Chemistry or equivalent
Job Purpose
To perform analytical testing, method development/optimization, method validation, and routine analysis of raw materials, in-process samples, finished products, and other samples in accordance with approved procedures, quality standards, and applicable regulatory requirements.
Key Responsibilities

  • Perform analytical testing of raw materials, intermediates, finished products, and stability samples as per approved methods and specifications.
  • Execute HPLC, GC, UV-Visible Spectrophotometer, FTIR, dissolution, pH, moisture/LOD and other applicable analytical techniques.
  • Support analytical method development, optimization, and method transfer activities.
  • Perform analytical method validation/verification as per applicable guidelines and internal procedures.
  • Prepare and maintain analytical solutions, reagents, mobile phases, standards, and reference materials.
  • Operate analytical instruments and ensure proper instrument usage, calibration, and maintenance.
  • Review analytical results and ensure accurate documentation of observations, calculations, chromatograms, and test results.
  • Investigate OOS/OOT results and support laboratory investigations and CAPA activities.
  • Maintain laboratory records, worksheets, logbooks, and analytical reports in accordance with GLP/GMP and SOP requirements.
  • Coordinate with QA, QC, Production, R&D, and other relevant departments for analytical requirements.
  • Support preparation and review of analytical protocols, reports, specifications, and SOPs.
  • Ensure proper handling, labeling, storage, and disposal of samples and chemicals.
  • Maintain laboratory housekeeping and comply with all applicable EHS and safety requirements.
  • Participate in internal/external audits and provide required analytical documentation.
  • Stay updated with current analytical techniques, regulatory requirements, and laboratory practices.

Required Technical Skills

  • Good knowledge of analytical chemistry and pharmaceutical/chemical analysis.
  • Hands‑on experience with HPLC and other analytical instruments.
  • Knowledge of chromatographic principles and analytical calculations.
  • Understanding of method validation parameters such as accuracy, precision, specificity, linearity, range, robustness, LOD, and LOQ.
  • Basic understanding of GMP, GLP, data integrity, and documentation practices.
  • Ability to interpret chromatograms and analytical data.
  • Good working knowledge of MS Excel and analytical documentation.
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