CQV Engineer - Transforming Pharma Systems & Validation

Process Automation – Controls.Instruments.Validations, Inc. is seeking a CQV Engineer to join our Indianapolis, IN team. In this role, you'll support the commissioning, qualification, and validation of manufacturing systems within regulated pharmaceutical environments, working on capital projects that transform complex systems into compliant, production-ready assets. Your responsibilities will include developing C&Q deliverables and ensuring regulatory compliance. A Bachelor's degree in Biomedical or Chemical Engineering and experience with CQV activities are required. Join us and make a measurable impact in critical manufacturing operations. #J-18808-Ljbffr