Validation Engineer

Computer System Validation (CSV)

Location:

Experience:

Industry:

Employment Type:

What You’ll Be Doing:

• Spearheading

  Computer System Validation (CSV) activities

  for pharmaceutical software & systems.
• Authoring and executing

  qualification protocols

  for GxP-regulated computerized systems.
• Ensuring compliance with

  FDA 21 CFR Part 11, EU Annex 11, GAMP 5, and Data Integrity

  guidelines.
• Reviewing and preparing key validation documents:

  URS, FRS, RTM, Test Scripts, and Final Validation Reports

  .
• Collaborating with cross-functional teams—

  QA, IT, Production, Automation, and Manufacturing

  —to drive compliance.

What We’re Looking For:

Engineering, Life Sciences, Computer Science, or related fields

pharmaceutical CSV projects

GxP, Data Integrity, and Good Documentation Practices (GDP)

✅ Excellent problem-solving, analytical, and documentation skills.

✅ Ability to manage multiple projects in a fast-paced, compliance-driven environment.

Ready to Apply?

Send your CV to hiring@arizonaautomationtech.com or reach out at +91 886-631-0370

🔹 Be part of a team that ensures compliance and innovation go hand in hand!