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Validation Engineer

Kenosha, Wisconsin

Piper Companies Logo

Job Id:
155943

Job Category:

Job Location:
Kenosha, Wisconsin

Security Clearance:
No Clearance

Business Unit:
Piper Companies

Division:
Piper Clinical Solutions

Position Owner:
Colin LaCroix

Piper Companies is hiring a skilled Validation Engineer for an onsite, contract position based out of Kenosha, Wisconsin. The Validation Engineer will be responsible for planning, executing, and documenting validation activities for equipment, utilities, and facilities to ensure compliance with regulatory and quality standards. 

  

Responsibilities of the Validation Engineer

  • Execute and document validation activities for equipment, utilities, and facilities in compliance with regulatory standards. 
  • Develop and maintain validation protocols, reports, and related documentation using Kneat and paper-based systems. 
  • Collaborate with cross-functional teams to ensure timely completion of validation deliverables. 
  • Support troubleshooting and resolution of validation-related issues during project execution. 
  • Ensure adherence to company quality standards and regulatory requirements throughout all validation processes. 

Qualifications for the Validation Engineer

  • 2–5 years of experience in parenteral manufacturing and commissioning & qualification (C&Q). 
  • Strong understanding of utilities and facilities within a regulated environment. 
  • Proficiency with Kneat systems (50/50 Kneat and paper-based environment). 
  • Solid knowledge of validation principles, GMP, and regulatory compliance. 
  • Excellent problem-solving and analytical skills with attention to detail. 

  

Compensation for the Validation Engineer

  •  Salary: $110,000-$125,000/year (USD) 
  • Benefits: Medical, Dental, Vision, sick leave if required by law, and 401K 

  

Keywords: Validation Engineer, Commissioning and Qualification, C&Q, Parenteral Manufacturing, GMP, Kneat, Validation Protocols, Utilities Validation, Facilities Validation, Clean Utilities, Dirty Utilities, Equipment Validation, Process Validation, Regulated Environment, Pharmaceutical Manufacturing, FDA Compliance, Quality Assurance, Validation Documentation, Paper-Based Validation, Project Management, Facility Work, Site Work 

#LI-CL1 

 

This job opens for applications on 12/5/25. Applications for this job will be accepted for at least 30 days from the posting date. 

 

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