CQV Engineer (Indianapolis, IN)
Indianapolis, IN
Job Id:
148400
Job Category:
Job Location:
Indianapolis, IN
Security Clearance:
No Clearance
Business Unit:
Piper Companies
Division:
Piper Clinical Solutions
Position Owner:
Peter Buechner
Piper Companies is searching for an experienced CQV Engineer to manage the commissioning, qualification and validation of equipment, systems, and processes to meet regulatory standards. The CQV engineer will be onsite in Indianapolis, IN.
Responsibilities for the CQV Engineer include:
· Execute Installation and Operational Qualification (IOQ) protocols for a Aseptic Filler system.
· Perform airflow testing and support potential design qualification activities.
· Collaborate with project teams to ensure compliance with CQV standards in a parenteral manufacturing environment.
· Support documentation and reporting of qualification activities, with Performance Qualification (PQ) potentially added to scope.
Requirements for the CQV Engineer include:
· Perform IOQ execution, airflow testing, and support design qualification in a parenteral manufacturing environment.
· Apply CQV principles to ensure equipment meets regulatory and operational standards, with potential involvement in future PQ activities.
· Collaborate with cross-functional teams to troubleshoot issues and maintain compliance throughout the commissioning process.
· Utilize technical documentation and validation protocols to support project deliverables and ensure traceability.
· Requires skills in GMP compliance, aseptic processing, technical writing, problem-solving, and familiarity with pharmaceutical manufacturing systems.
Compensation for the CQV Engineer includes:
· Salary: $75,000 - $100,000 based on experience
· Comprehensive benefits: Medical, Dental, Vision, 401k, PTO, holidays, and sick leave as required by law.
This job is open for applications on 8/11/2025. Applications for this job will be accepted for at least 30 days from the posting date.
Keywords: CQV engineer, qualification, IQ, OQ, PQ, validation, GMP, good manufacturing practices, cGMP compliance, FDA regulation, ISO standards, quality system regulation, QSR, risk assessment, equipment validation, process validation, cleanroom protocols, automation system, calibration, trackwise, problem solving, technical writing, communication, adaptability, time management
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