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Validation Intern

The Validation Intern will assist the Validation Department in maintaining compliance with GMP standards across equipment, facility, and computerized systems. This internship provides broad exposure to core validation disciplines— including cleaning validation, computer system validation (CSV), and process validation—while developing practical skills in data analysis, documentation, and system management within a regulated pharmaceutical environment.

Key Responsibilities:

  • Collect, organize, and analyze data from environmental monitoring and validation activities.
  • Support drafting, sorting, and archival of validation documents per GDP (Good Documentation Practice) requirements.
  • Assist in maintaining equipment and instrument inventories, traceability matrices, and document templates within the electronic quality management system (e.g., Valgenesis, TrackWise, Documentum etc.).
  • Review and update facility, equipment, and critical utility storyboards to ensure alignment with current configurations.
  • Participate in execution of equipment qualification and cleaning validation protocols under supervision of senior validation staff.
  • Provide support in developing and reviewing cleaning validation documentation, including sampling plans and acceptance criteria.
  • Assist with computer system validation activities such as user requirement specifications, test scripts, and validation summary reports.
  • Observe and contribute to process validation activities, including protocol preparation, data trending, and deviation evaluation.
  • Collaborate with Engineering, Quality Control, and Manufacturing teams to support cross-functional validation projects.

Learning Outcomes:

Interns will gain practical understanding of validation lifecycle management, including cleaning, equipment, process, and computer system validation. They will develop core skills in regulated documentation, data integrity, and GMP compliance—essential foundations for a career in pharmaceutical validation or quality assurance.

 

Please note that all resumes will be accepted only until April 1, 2026.