Piper Companies
Piper Companies
is seeking a
CQV Engineer
based in the
RTP (NC) . This
CQV Engineer
will be responsible for ensuring that pharmaceutical manufacturing equipment, systems, and processes are properly commissioned, qualified, and validated in compliance with regulatory and quality standards.
Responsibilities of the CQV Engineer
Develop and execute protocols (IQ/OQ/PQ) for equipment, utilities, and systems to ensure compliance with regulatory standards.
Support commissioning activities, including system walkdowns, punch list resolution, and functional testing.
Collaborate with cross-functional teams (engineering, quality, manufacturing) to ensure timely project delivery and alignment with GMP requirements.
Generate and review documentation, such as validation plans, reports, and SOPs.
Troubleshoot and resolve issues during qualification and validation phases to maintain project timelines.
Qualifications for the CQV Engineer
5+ years of related experience.
Strong understanding of IOQ protocol development, execution, and component-level assessments.
Ability to work cross-functionally with QA, engineering, and external vendors.
Bachelor's degree in chemical, mechanical, or similar engineering degree.
Compensation for the CQV Engineer
Salary Range : $105,000 – $125,000/year
Comprehensive Benefits : Sick leave if required by law, medical, dental, vision, 401K
This job opens for applications on 10/13/2025. Applications for this job will be accepted for at least 30 days from the posting date.
Keywords : CQV Engineer, Commissioning, Qualification, Validation, GMP, FDA, IQ OQ PQ, Cleanroom, Biotech, Pharmaceutical, Equipment Validation, Process Validation, Utilities, SOP Development, Risk Assessment, Deviation Management, CAPA, Life Sciences, Engineering, Chemical Engineering, Mechanical Engineering, Biomedical Engineering, Validation Protocols, Regulatory Compliance, CSV, Automation, Quality Systems, Project Engineering, cGMP, FDA 21 CFR Part 11, GAMP 5
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is seeking a
CQV Engineer
based in the
RTP (NC) . This
CQV Engineer
will be responsible for ensuring that pharmaceutical manufacturing equipment, systems, and processes are properly commissioned, qualified, and validated in compliance with regulatory and quality standards.
Responsibilities of the CQV Engineer
Develop and execute protocols (IQ/OQ/PQ) for equipment, utilities, and systems to ensure compliance with regulatory standards.
Support commissioning activities, including system walkdowns, punch list resolution, and functional testing.
Collaborate with cross-functional teams (engineering, quality, manufacturing) to ensure timely project delivery and alignment with GMP requirements.
Generate and review documentation, such as validation plans, reports, and SOPs.
Troubleshoot and resolve issues during qualification and validation phases to maintain project timelines.
Qualifications for the CQV Engineer
5+ years of related experience.
Strong understanding of IOQ protocol development, execution, and component-level assessments.
Ability to work cross-functionally with QA, engineering, and external vendors.
Bachelor's degree in chemical, mechanical, or similar engineering degree.
Compensation for the CQV Engineer
Salary Range : $105,000 – $125,000/year
Comprehensive Benefits : Sick leave if required by law, medical, dental, vision, 401K
This job opens for applications on 10/13/2025. Applications for this job will be accepted for at least 30 days from the posting date.
Keywords : CQV Engineer, Commissioning, Qualification, Validation, GMP, FDA, IQ OQ PQ, Cleanroom, Biotech, Pharmaceutical, Equipment Validation, Process Validation, Utilities, SOP Development, Risk Assessment, Deviation Management, CAPA, Life Sciences, Engineering, Chemical Engineering, Mechanical Engineering, Biomedical Engineering, Validation Protocols, Regulatory Compliance, CSV, Automation, Quality Systems, Project Engineering, cGMP, FDA 21 CFR Part 11, GAMP 5
#LI-GP2
#J-18808-Ljbffr