Piper Companies
Piper Companies
is looking for a
Validation Engineer II
to join acommercial-stage pharmaceutical company focused on organ manufacturing and transplantlocated 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 #LI-MU1 #LI-ONSITE
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is looking for a
Validation Engineer II
to join acommercial-stage pharmaceutical company focused on organ manufacturing and transplantlocated 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 #LI-MU1 #LI-ONSITE
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