Validation Engineer II

Piper Companies is looking for a Validation Engineer II to join a commercial-stage pharmaceutical company focused on organ manufacturing and transplant located in Silver Spring, Maryland.

Responsibilities of the Validation Engineer II include:

· Carry out hands-on testing and qualification of equipment used in manufacturing and cleanroom environments

· Run and document validation protocols (IQ/OQ/PQ) for sterilization systems and related machinery

· Work directly with systems like autoclaves, SIP (Steam-in-Place), CIP (Clean-in-Place), and dry heat sterilizers to ensure proper function and compliance

· Perform temperature mapping and other studies to verify equipment performance

· Partner with teams across engineering, manufacturing, and quality to keep projects on track and compliant

· Help prepare for inspections by organizing validation records and offering technical insights

Qualifications for the Validation Engineer II include:

· Bachelor’s degree in engineering, life sciences, or a related discipline

· 3–7+ years of experience in validation within the pharmaceutical or biotech industry

· Strong hands-on background with sterilization systems including SIP, CIP, autoclaves, and dry heat

· Solid grasp of IQ (Installation Qualification), OQ (Operational Qualification), and PQ (Performance Qualification) processes

· Able to work independently and take initiative with minimal guidance

· Detail-oriented with strong documentation and organizational skills

· Comfortable working in a fast-paced environment and responding quickly to project needs

Compensation for Validation Engineer II includes:

· Salary Range: $80,000–$110,000

· Comprehensive Benefit Package: Cigna Medical/Dental/Vision, 401K, Sick Leave as Required by Law

This job is open for applications on 8/11/2025. Applications will be accepted at least 30 days from the posting date

Keywords: Validation Engineer, GMP, Good Manufacturing Practice, IQ, Installation Qualification, OQ, Operational Qualification, PQ, Performance Qualification, SIP, Steam-in-Place, CIP, Clean-in-Place, Autoclaves, Dry Heat Sterilization, Pharmaceutical, Biopharmaceutical, Equipment Qualification, Process Validation, Temperature Mapping, FDA, Food and Drug Administration, QA, Quality Assurance, Engineering, Manufacturing, Contract-to-Hire, Silver Spring, Maryland, Life Sciences, Equipment Validation, Sterilization Systems, Cleanroom, Biotech, Validation Lifecycle, Technical Documentation, Audit Support, Cross-functional Collaboration, First Shift, Fast-Paced Environment

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