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Company Contact Info

  • Raleigh, NC
  • Experis

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Validation Engineer

Experis • Raleigh, NC

Posted 11 days ago

Job Snapshot

Full-Time
Manufacturing, Other Great Industries, Pharmaceutical
Manufacturing, Pharmaceutical, Science

Job Description

Responsibilities for Validation Engineer:


  • Manage, coordinate and oversee all validation studies, cleaning validation, change controls, protocol revisions, equipment validation, and documentation of results for manufacturing equipment including, but not limited to, filling and packaging lines, autoclaves, washers, and formulation tanks.

  • Oversee compliance to compliance to company policies and procedures, GMP and GLP regulations, and validation protocols.
  • Lead, mentor, and train junior validation engineers.
    Complete validation reports, write summaries of work, and perform statistical analyses.

Technical Requirements for Senior Validation Engineer:

  • Bachelors Degree in Engineering or related scientific field.

  • Minimum 6 years of experience in a GMP regulated pharmaceutical manufacturing environment.
  • Extensive knowledge of Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).
  • Experience with thermal validation and environmental monitoring equipment, including ValProbe, swabs and plates, and Kaye.
    Computer system validation experience a plus.

Compensation & Benefits for Senior Validation Engineer:


  • Compensation: based on previous salary history and experience

  • Full Benefits: Medical, Dental, Vision, 401k, PTO

We offer all the advantages you would expect from an industry leader - including a competitive salary, health, dental and vision insurance, paid holidays, training and more!

We've got the right opportunity. Tell us why you're the right person! Apply today @ [Click Here to Email Your Resumé].

Experis is an Equal Opportunity Employer (EOE/AA)

Job ID: FOX_11327093
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