Validation Engineer

  • Location: Omaha, Nebraska
  • Type: Direct Hire
  • Job #18490

Validation Engineer
Location: Omaha, NE

Dive into the heart of innovation with a career opportunity at a leading pharmaceutical manufacturer! As a Validation Engineer, you’re not just filling a role; you’re stepping into a pivotal position where your work directly contributes to the development and optimization of products that impact lives globally. This is your chance to join a team where diverse ideas bloom, learning is fast-paced, and your impact is immediate and valued. Be part of a culture that thrives on collaboration, excellence, and respect, all while pushing the boundaries of what’s possible in the pharmaceutical industry.
Why You Should Apply

  • Be a part of a pioneering team dedicated to improving global health through innovation.
  • Engage in meaningful work that offers rapid learning and personal growth opportunities.
  • Competitive compensation package, including salary, bonus, and comprehensive benefits.
  • Family-friendly benefits with 100% company-paid premiums for medical, dental, and vision.
  • 401k with company match, wellness incentives, and a supportive, dynamic work environment.

What You’ll Be Doing

  • Troubleshoot operations and processing issues through lab-scale processing and data analysis.
  • Develop and optimize products for internal and external production.
  • Lead Change Controls, Deviation investigations, and CAPA initiatives efficiently.
  • Execute qualification/validation protocols (IQ, OQ, PQ, PV) and generate related reports.
  • Support the Validation Master Plan and Calibration program in compliance with cGMPs.
  • Facilitate the improvement and revision of SOPs, Manufacturing Instructions, and documentation.

About You

  • Be able to do the job as described.
  • Bachelor’s degree in a Science related field, with a preference for advanced degrees.
  • Minimum of 3 years qualification/validation experience in a regulated industry.
  • Knowledge of US FDA 21 CFR Part 117 and Q7 cGMP requirements.
  • Strong organizational, communication, and computer skills (Windows applications).

How To Apply
We’d love to see your resume, but we don’t need it to have a conversation. Send us an email to and tell me why you’re interested. Or, feel free to email your resume. Please include Job#18490.