Validation Engineer

Piper Companies is seeking a Validation Engineer to join a leading pharmaceutical project in Kenosha, Wisconsin. This role supports a major site expansion, with multiple projects focused on utilities and facilities within a regulated environment. The Validation Engineer will play a key role in commissioning, qualification, and validation (CQV) activities, ensuring compliance and operational excellence in a dynamic setting.

This position is onsite and offers a temp-to-hire opportunity, with long-term work projected for approximately five years. The first project runs through May or June, with additional projects to follow.

Responsibilities of the Validation Engineer:

• Execute CQV activities for utilities and facilities in a regulated environment.
• Support commissioning and qualification efforts for parenteral manufacturing processes.
• Work within a 50/50 Kneat and paper-based documentation environment.
• Collaborate with project teams to ensure compliance with regulatory standards.
• Maintain high standards of quality and documentation throughout all validation processes.

Qualifications of the Validation Engineer:

• 5+ years of experience in parenteral manufacturing and C&Q.
• Strong background in regulated environments.
• Kneat experience is required.
• Bonus experience in: Project management, clean utilities, dirty utilities, facility work, or site work.
• Excellent communication and organizational skills.

Compensation & Benefits for the Validation Engineer:

• Competitive hourly rate: $50–$57/hr, based on experience.
• Full benefits including health, dental, vision, and 401k.
• Temp-to-hire opportunity with long-term project stability.

Key Words:

Validation Engineer, CQV, Kneat, Commissioning, Qualification, Utilities, Facilities, Parenteral Manufacturing, cGMP Compliance, Paper-Based Documentation, Site Expansion, Pharmaceutical Validation, Project Management, Clean Utilities, Dirty Utilities, Temp-to-Hire, Regulated Environment

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