PACIV, an international control systems integration and regulatory compliance engineering firm servicing Bio-Pharmaceutical, Medical Device, F&B, and Water/Wastewater clients, is looking for a full-time Validation Engineer (Level I) team member for our USA office (Indianapolis).       Job Description: The Validation Engineer will manage various commissioning, qualification, and/or validation facets within our client’s Biotechnology and Pharmaceutical sites.  This support service will work within the client’s validation, project management, quality, and/or automation department team(s).    Position Responsibilities/Essential Functions + + Develop and/or drive to completion the following Commissioning and Qualification (C&Q) deliverables: project validation plan, risk assessments and project strategies, requirements, functional design specifications, software/hardware design specifications, impact assessments, trace matrix, test cases/scripts, engineering studies, and summary reports. + Thoroughly understand the commissioning and qualification process and influence cross-functional team members to ensure adherence to governing policy and procedure. + Ensure change management is properly assessed throughout the course of the project and all documentation impacted is maintained.  This includes changes due to evolving design and failures during test execution.    + Lead and participate in project review meetings such as design reviews, alignment sessions, test strategy, test execution reviews, project status, and qualification review meetings. + Manage and report project scope and budget considerations as it relate to C&Q. + Develop and maintain documentation within an electronic lifecycle management system capable of paperless execution. + Support the execution of large capital projects that contribute to the expansion of pharmaceutical manufacturing.  Projects may include the following types of equipment: active pharmaceutical ingredient manufacturing, filling operations, delivery device assembly, packaging, facilities and utilities, and automation. Requirements + + Bachelor’s degree in engineering or a technical discipline required + 2+ years of validation experience in the Pharmaceutical Industry + Comfortable with a 24/7 manufacturing environment + Works well with others within a team and takes accountability + Can handle a high-pressure, high-stress work environment + Result-driven and self-motivated + Strong interpersonal and communication skills (verbal and presentation) + Organized with strong computer literacy, such as MS Word, Project, Excel, etc. Desired Hard Skill Sets (via Internships/Co-Ops): + + Familiarity with Validation principles and executable deliverables (i.e. Requirements, Design, Testing, Reports, etc.) + C&Q and/or CSV experience, ideally around Data Integrity and CFR Part 11 Electronic Records and Signatures + Project Management experience with the ability to lead and drive projects to completion autonomously Other Requirements Location:  Indianapolis Travel: Up to 40% of the time to various suppliers, collaborators, and client sites outside of Indianapolis Powered by JazzHR