Validation Analyst
Validation Documentation
- LocationNoida, Uttar Pradesh, India
- Work modeOn-site
- TypeFull-time
- Experience0–5 years required
- SalaryNot disclosed
Veeva, Gamp 5, Validation Plan, Iq/oq/pq, Audit Trail
Overview
This role involves creating and maintaining validation documentation for pharma clients using Veeva platforms. The candidate will author validation plans, execute OQ/PQ scripts, and ensure compliance with GAMP 5 standards. They will work closely with cross-functional teams to support audit readiness and manage deviations.
Summarised by InternDoor from Axtria - Ingenious Insights’s posting, in our own words. The posting itself is the source of truth, so check it before you apply.
Responsibilities
- Review and document validation evidence for Veeva platform configurations
- Author validation plans and reports for pharma compliance
- Collaborate with QA and compliance teams on audit readiness
Requirements
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How to apply
- Check what they ask for. Read the requirements above: Axtria - Ingenious Insights asks for 0–5 years.
- Tailor your resume to the role. Put the work that matches these skills first. InternDoor’s resume tailor does it against this posting.
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Application details
- Posted
- , on LinkedIn
- First seen by InternDoor
- , within 13 minutes of being posted
- Last checked
- : the posting was still in LinkedIn’s search results. We have not checked its application page.
- Application deadline
- Axtria - Ingenious Insights has not stated one
- Leaves InternDoor
- By , our 30-day limit for LinkedIn listings, or sooner if the application closes
- Application page
- career10.successfactors.com
What we checked, and what the dates mean
The date this listing leaves InternDoor is our own rule, not a deadline set by Axtria - Ingenious Insights. Postings can close earlier, at any time.
InternDoor has recorded 4 engineering postings from Axtria - Ingenious Insights in India since Sept 2026.
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