Officer/ Sr Officer R&D ADL

Troikaa Pharmaceuticals; Ahmedabad District; On-site; INR 600,000 - 900,000; Full time

Job summary

Troikaa Pharmaceuticals in Ahmedabad is seeking an experienced analytical chemist to lead HPLC method development and validation for APIs/formulations. The role requires hands-on work with GC, UV spectrophotometry, and Karl Fischer, ensuring accurate analysis of drug substances and impurities.

You will prepare SOPs, STPs, and specifications, review technical reports, and ensure compliance with GMP and EHS regulations in every analytical activity.

Qualifications

• Strong knowledge of HPLC method development and validation for APIs/formulations.
• Experience in characterization of drug substances and intermediates.
• Preparation and review of SOPs, STPs, and specifications.
• Hands-on experience with GC, UV spectrophotometer, Auto Titrator, Karl Fischer.
• Knowledge of ion chromatography for ionic impurities.

Responsibilities

• Strong practical knowledge of HPLC method development and validation for assay and related substances of APIs/Formulations.
• Experience in characterization of drug substances, including intermediates, in-process materials, stability samples, and unknown impurities.
• Preparation and review of SOPs, STPs, and specifications.
• Hands-on experience with analytical instruments such as GC, UV spectrophotometer, Auto Titrator, Karl Fischer, etc.
• Knowledge of ion chromatography for analysis of ionic impurities in drug substances.
• Preparation of technical documents and reports, including AMDR, protocols, justification reports, and analytical reports.
• Ensure adherence to GMP, SOPs, and EHS regulations.

Skills

HPLC method development

Method validation

SOP writing

GMP awareness

Analytical thinking

Tools

Gas Chromatography

UV Spectrophotometer

Auto Titrator

Karl Fischer

Ion Chromatography

Job description

Role & responsibilities

• Strong practical knowledge of HPLC method development and validation for assay and related substances of Active Pharmaceutical Ingredients/Formulations.
• Experience in characterization of drug substances, including intermediates, in-process materials, stability samples, and unknown impurities (identification/confirmation).
• Preparation and review of SOPs, STPs, and specifications.
• Hands-on experience with analytical instruments such as Gas Chromatography (GC), UV Spectrophotometer, Auto Titrator, Karl Fischer, etc.
• Knowledge of ion chromatography for analysis of ionic impurities in drug substances.
• Preparation of technical documents and reports, including AMDR, protocols, justification reports, and analytical reports.
• Ensure adherence to GMP, SOPs, and EHS (Environment, Health & Safety) regulations.