Validation engineer_ cGMP, FDA, Emerson DeltaV_w2

360 IT ProfessionalsAndover, MA🇺🇸United StatesPosted Jun 29, 2017

Why This Role Stands Out

This role offers a fantastic opportunity to leverage your cGMP, FDA, and Emerson DeltaV expertise within a reputable IT services company, contributing to impactful technology solutions for global clients. If you are a mid-senior level validation engineer with a strong background in regulated environments and a knack for instrument validation, you will thrive in this position. Apply now to advance your career and make a significant contribution.

Quick Overview

Seniority

Mid Senior

Employment type

Contract

Work mode

On Site

Location

Andover, MA, United States

Posted

9 years ago

Job Description

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

• 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

In person interview is acceptable.