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QC Chemist

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Onsite

QC Chemist

Levantex Pharmaceuticals

QC Chemist

Skills

RComplianceRegulatory Compliance

3 months ago

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Important information


Contract type:

Permanent

Location:

Solapur, Maharashtra, India

Work mode:

Onsite

Published on:

8 August 2026

What they need


About the Role

We are looking for an experienced and detail-oriented QC Chemist to join our pharmaceutical intermediates manufacturing facility. The candidate will be responsible for testing raw materials, in-process samples and finished products, ensuring that all materials meet the required quality specifications.

Key Responsibilities

  • Perform chemical analysis of raw materials, in-process samples and finished products.
  • Conduct routine analysis using laboratory instruments and analytical techniques such as HPLC, GC, titration, moisture analysis and other wet chemistry methods.
  • Perform testing as per approved specifications, test methods and standard operating procedures (SOPs).
  • Prepare and maintain accurate laboratory records, analytical reports and test results.
  • Review analytical results and identify any out-of-specification (OOS) or abnormal results.
  • Coordinate with the Production and R&D teams regarding analytical results and process-related issues.
  • Assist in method development, method validation and method transfer where required.
  • Maintain proper calibration and routine checks of laboratory instruments.
  • Prepare and maintain reagents, solutions and laboratory standards.
  • Ensure proper sampling, labelling and storage of samples.
  • Follow laboratory safety procedures, GMP/GLP practices and company quality procedures.
  • Maintain cleanliness and proper housekeeping of the QC laboratory.
  • Assist in maintaining documentation required for audits and regulatory compliance

Qualifications

  • B.Sc. / M.Sc. in Chemistry.
  • M.Sc. Chemistry candidates will be preferred.
  • Candidates with relevant experience in pharmaceutical intermediates, API, speciality chemicals or fine chemicals will be preferred.

Experience

  • 27 years of relevant experience in Quality Control / Analytical Chemistry.
  • Experience in a pharmaceutical, API, pharmaceutical-intermediate or chemical manufacturing environment is preferred

Desired Skills

  • Good practical knowledge of HPLC and GC.
  • Strong understanding of analytical chemistry and wet chemistry techniques.
  • Ability to interpret chromatograms and analytical results.
  • Knowledge of laboratory documentation and SOPs
  • Good attention to detail and record-keeping skills.
  • Ability to work independently and coordinate effectively with Production and R&D teams.

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