Validation Engineer
4 days ago
Are you ready to take your career to the next level in
Computer System Validation (CSV)
? Join us at
Arizona Automation & Technologies
, where we ensure compliance, quality, and innovation in pharmaceutical technology.
Location:
PAN INDIA
Experience:
4-7 Years
Industry:
Pharmaceutical / Life Sciences
Employment Type:
Full-time
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:
Bachelor's degree in
Engineering, Life Sciences, Computer Science, or related fields
.
Hands-on experience in
pharmaceutical CSV projects
(LIMS, MES, ERP, etc.) will be an advantage.
Strong knowledge of
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 or reach out at
Be part of a team that ensures compliance and innovation go hand in hand
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