Validation Engineer (330800)

IDR is seeking a

CSV Specialist

to join one of our top clients on an

Onsite

schedule. If you are looking for an opportunity to join a large organization and work within an ever-growing team-oriented culture, please apply today!

Position Overview for the CSV Specialist:
A dedicated and detail-oriented CSV Specialist is required for an on-site position to ensure the integrity and compliance of computerized systems within pharmaceutical manufacturing. The specialist will be responsible for the validation of Enterprise IT systems, standalone laboratory and manufacturing equipment, maintaining audit readiness and experience with audit trail review programs.

Required Skills for the CSV Specialist:
Must have hands-on experience validating standalone equipment, instruments, around existing IT Infrastructure, lab, and manufacturing systems.
3+ years' working experience in validation or QA role
1+ year of experience with Delta V automation
Experience with any MES (Manufacturing execution system)
Must have hands on working experience with a QMS Systems like Veeva or Track Wise
Expert level experience in CSV Documentation
Experience in computer system validation within the pharmaceutical manufacturing industry.
In-depth knowledge of GxP, 21 CFR Part 11, and other relevant regulatory guidelines.
What's in it for you?
Competitive compensation package
Full Benefits; Medical, Vision, Dental, and more!
Opportunity to get in with an industry leading organization
Close-knit and team-oriented culture
Why IDR?
20+ Years of Proven Industry Experience in 4 major markets
Medical, Dental, Vision, and Life Insurance
ClearlyRated's Best of Staffing Client and Talent Award winner 10 years in a row

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