Quality Control (IP)

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Quality Control (IP)

work outline icon0 - 5 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Aurobindo Pharma Limited

time outline iconJadcherla, Telangana, India

Posted on 20-03-2025

1 Vacancy

Description

  • Perform physical, chemical, and microbiological testing of raw materials, in-process samples, and finished products.
  • Ensure adherence to Good Laboratory Practices (GLP) and industry guidelines.
  • Conduct stability studies and validation of analytical methods.
  • Maintain accurate records of test results, reports, and certificates of analysis (CoA).
  • Perform HPLC, GC, UV Spectroscopy, FTIR, and other analytical techniques.
  • Document and investigate Out of Specification (OOS) and Out of Trend (OOT) results.
  • Ensure compliance with GMP, FDA, WHO, ISO, and other regulatory requirements.
  • Prepare for internal & external audits by maintaining proper records and quality reports.
  • Implement corrective & preventive actions (CAPA) based on audit findings.

Category

Pharmaceuticals

Functional Area

Pharma Quality Control (QC)

Preferred Education

BSc (Bachelor of Science)BPharm (Bachelor Of Pharmacy)

Key Skills

Attention to DetailCommunicationTeam WorkPositive Attitude

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