Executive - Bioanalytical

Torrent Pharmaceuticals

Ahmedabad District

On-site

INR 350,000 - 520,000

Full time

14 days+

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Job summary

Torrent Pharmaceuticals in India seeks a qualified Analyst to develop and validate sensitive bioanalytical methods using LCMS/HPLC, and to independently conduct BA/BE sample analysis with accuracy. The candidate will maintain and calibrate instruments in aGDP/GLP governed lab, ensuring compliance with regulatory requirements.

MSC/M.Pharm candidates with hands-on experience in bioanalysis are encouraged to apply; the role emphasizes strict adherence to SOPs, method validation, and quality systems

Qualifications

  • Develop and validate sensitive bioanalytical methods using extractions (SPE, LLE) and quantitation (LCMS, HPLC).
  • Conduct sample analysis for Bioavailability/Bioequivalence studies independently with accuracy.
  • Operate, maintain and calibrate laboratory instruments following SOPs.
  • Ensure GDP and GLP compliance in the laboratory and stay aligned with regulatory requirements.

Responsibilities

  • Develop and validate bioanalytical methods for drug substances using SPE, LLE, LCMS/HPLC.
  • Perform independent BA/BE sample analysis with precise results.
  • Maintain and calibrate instruments, adhering to written procedures.
  • Ensure GDP/GLP compliance and awareness of regulatory requirements.

Skills

Bioanalytical methods
LCMS/HPLC
Bioavailability studies
GLP/GDP compliance
Instrument maintenance

Education

MSc/M.Pharm

Tools

LCMS
HPLC

Job description

Analyst:


  • Experience in developing and validating sensitive and rugged bioanalytical methods by using different extractions (i.e. SPE, LLE etc.) and quantitation (i.e. LCMS, HPLC) techniques for analysis of drug substances

  • Experience in conducting sample analysis of Bioavailability/Bioequivalence Studies independently with required accuracy.

  • Experience in operation, maintenance and calibration of laboratory instruments adhering to written instrument operation procedures.

  • Ability to maintain GDP and GLP compliance in the laboratory.

  • Know-how of current applicable regulatory requirements.


Qualification:

MSC/ M. Pharm

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