Posted:1 day ago| Platform: Foundit logo

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Work Mode

On-site

Job Type

Full Time

Job Description

  • Analyze various pharmaceutical materials including:
  • In-process samples
  • Intermediates
  • Raw materials
  • Packing materials
  • Finished products
  • Stability study samples
  • Hold time study samples
  • Process validation samples
  • Cleaning samples
  • Vendor development samples
  • Any other analysis allocated by the team leader.
  • Release analytical results with proper documentation.
  • Take responsibility for ensuring the quality and purity of pharmaceutical products using High-Performance Liquid Chromatography (HPLC) techniques.
  • Prepare samples for HPLC analysis according to established Standard Operating Procedures (SOPs) and specifications.
  • Analyze HPLC data, interpret results, and generate reports documenting test results and any deviations.
  • Ensure all analyses are performed in compliance with Good Laboratory Practices (GLP).
  • Ensure all raw analytical data is documented online.
  • Initiate, complete, and file daily analysis reports.
  • Ensure any abnormal results, incidents, deviations, or discrepancies are reported immediately to the reporting Section Head.
  • Ensure all relevant log entries are made for every activity wherever applicable.
  • Supervise compliance with all current Good Manufacturing Practices (cGMP), GxP, or any other regulatory requirements, including Environment, Health, and Safety (EHS) requirements.
  • Report any quality concerns or suggestions for improvements to the Department Head.
  • Execute and supervise all tasks and activities as per the applicable SOPs and company policy.
  • Maintain safety norms while working in the lab (e.g., wear goggles and Personal Protective Equipment (PPE), dispose of samples/media as per procedure, etc.).
  • Ensure analysis is performed according to valid procedures and by using calibrated instruments and standards.
  • Ensure self-discipline with respect to wearing aprons, attendance, personnel hygiene, and interpersonal relations.
  • Perform Labware Laboratory Information Management System (LIMS) related activities.
  • Handle any other assignments given by the Section Head or Department Head.

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Alembic Pharmaceuticals logo
Alembic Pharmaceuticals

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