Validation Engineer
Kenosha, Wisconsin
Job Id:
156387
Job Category:
Job Location:
Kenosha, Wisconsin
Security Clearance:
No Clearance
Business Unit:
Piper Companies
Division:
Piper Clinical Solutions
Position Owner:
Gray Young
Piper Companies is seeking an experienced Validation Engineer for an onsite, contract role in Kenosha, Wisconsin. This position involves planning, executing, and documenting validation activities for equipment, utilities, and facilities to ensure compliance with regulatory and quality standards.
Key Responsibilities
- Perform and document validation activities for equipment, utilities, and facilities in accordance with regulatory requirements.
- Develop and maintain validation protocols, reports, and related documentation using both Kneat and paper-based systems.
- Collaborate with cross-functional teams to ensure timely delivery of validation milestones.
- Troubleshoot and resolve validation-related issues during project execution.
- Maintain strict adherence to company quality standards and regulatory guidelines throughout all validation processes.
Required Qualifications
- 2–5 years of experience in parenteral manufacturing and commissioning & qualification (C&Q).
- Strong understanding of utilities and facilities in a regulated environment.
- Proficiency with Kneat systems (approximately 50/50 Kneat and paper-based documentation).
- Solid knowledge of validation principles, GMP, and regulatory compliance.
- Excellent analytical and problem-solving skills with strong attention to detail.
Compensation & Benefits
- Salary: $110,000–$125,000 annually
- Benefits: Medical, Dental, Vision, sick leave (as required by law), and 401(k)
This application opens 12/1/25 and will remain open for at least 30 days from the posting date.
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-GY1 #LI-ONSITE #PANDO