Posted 3 months ago
Validation engineer_ cGMP, FDA, Emerson DeltaV_w2
AI Summary
A validation engineer performs validation of utilities and equipment in cGMP environments, focusing on IQ/OQ protocols, CIP/SIP cycles, and compliance with FDA regulations.
About this role
Validation engineer_ cGMP, FDA, Emerson DeltaV_w2
360 IT Professionals is a Software Development Company based in Fremont, California that offers complete technology services in Mobile development, Web development, Cloud computing and IT staffing. Merging Information Technology skills in all its services and operations, the company caters to its globally positioned clients by providing dynamic feasible IT solutions. 360 IT Professionals work along with its clients to deliver high-performance results, based exclusively on the one of a kind requirement.
We are looking to fill a validation engineer in Andover MA
Qualifications
• 7 years of relevant utilities and equipment validation experience
• The candidate must have a strong background working in cGMP environments.
• The candidate must have excellent communication skills.
• Experience with Emerson Controllers and Emerson DeltaV Software is required.
• The ideal candidate would have experience with:
o CIP and SIP cycle development.
o Kaye Validator
o SIP Qualification w/ BI’s
o IQ, OQ and Instrument Validation
Additional Information
In person interview is acceptable.
Skills
Explore related jobs
More jobs at 360 IT Professionals
Browse these categories
Market data for this role
All reports →- SeriesRole reportsOne role family at a time: how many openings, what changed this week, who is hiring, what it pays.
- SeriesSalary reportsWhat employers publish in job postings, by level and workplace. Not self-reported pay.
- Market overviewState of tech hiring, September 2026: up 4.8%Tech hiring rose 4.8% month over month in September 2026, with 411,122 new listings. Customer support and account executive roles led the growth.