Posted:3 hours ago| Platform: Naukri logo

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Job Type

Full Time

Job Description

  • Prepare and review study protocols, reports, and SOPs
  • Ensure compliance with GLP, GDP, and regulatory guidelines
  • Collaborate with cross-functional teams for data collation
  • Maintain document version control and audit readiness
  • Ensure clarity, accuracy, and consistency in technical writing
  • Support regulatory submissions and internal audits
  • Review raw data for completeness and integrity
  • Track timelines to ensure on-time document delivery

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Amneal Pharmaceuticals logo
Amneal Pharmaceuticals

Pharmaceutical Manufacturing

Bridgewater New Jersey

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