Research Executive - Formulation Development Analytics (ADL)

Unichem Laboratories Ltd.

North Goa

On-site

INR 300,000 - 520,000

Full time

5 days ago
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Job summary

Unichem Laboratories Ltd. in Goa seeks an analytical professional to support validation and query responses for finished products.

You will validate analytical methods, prepare validation reports, and oversee general laboratory maintenance to ensure cGMP compliance. Key duties include routine and stability analyses (assay, impurities, dissolution, residual solvents), calibrating instruments (HPLC, GC, UV-Vis), troubleshooting, maintaining reference standards, and coordinating with Chemical and

Responsibilities

  • Perform analytical method validation and query response for the finished product.
  • Prepare analytical validation reports.
  • Monitoring general laboratory and its maintenance activity as applicable.
  • Responsible for performing routine analysis and stability analysis of the finished product for assay, CU, related substances, dissolution and residual solvent etc.
  • Prepare draft STP.
  • Review and compile stability data for finished product analysis.
  • Responsible for troubleshooting and maintenance of HPLC, GC, UV/Visible and spectrophotometer etc.
  • Calibration of analytical instruments as per the schedule.
  • Following in house systems and procedures to ensure cGMP practices and regulatory requirements.
  • Carry out literature survey by establishing the strategies
  • Maintenance of reference standard, working standards and their standardization.
  • Co-ordinating the activities in Chemical and Instrumentation.
  • Handling of Troubleshooting.

Job description

  • Perform analytical method validation and query response for the finished product.
  • Prepare analytical validation reports.
  • Monitoring general laboratory and its maintenance activity as applicable.
  • Responsible for performing routine analysis and stability analysis of thefinished product for assay, CU, related substances, dissolution and residual solvent etc.
  • Prepare draft STP.
  • Review and compile stability data for finished product analysis.
  • Responsible for troubleshooting and maintenance of HPLC, GC, UV/Visible and spectrophotometer etc.
  • Calibration of analytical instruments as per the schedule.
  • Following in house systems and procedures to ensure cGMP practices and regulatory requirements.
  • Carry out literature survey by establishing the strategies
  • Maintenance of reference standard, working standards and their standardization.
  • Co-ordinating the activities in Chemical and Instrumentation.
  • Handling of Troubleshooting.
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