6244 - CIP (Clean-in-Place) Engineer

Description Verista’s 500 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world’s most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities. Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day. Company Culture Guidelines & Values: We empower and support our colleagues We commit to client success at every turn We have the courage to do the right thing We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged. We constantly acquire new skills and learn from our experiences to enhance our collective expertise We are seeking a Clean-in-Place (CIP) Engineer with hands-on experience overseeing the commissioning and qualification of Clean-In-Place (CIP) systems. This role ensures that all systems are designed, tested, and documented in alignment with project requirements and safety standards. Clean-in-Place (CIP) Engineer Responsibilities: CIP System Leadership Serve as the commissioning and qualification (C&Q) lead for CIP systems (responsibilities described below). Develop and optimize CIP cleaning cycles to meet operational and quality standards. Supervise the safe introduction and handling of caustic solutions during cleaning cycle development. C&Q Lead Responsibilities Commissioning and Qualification Documentation Gain a thorough understanding of system design by reviewing engineering documentation, P&IDs, and design specifications. Develop User Requirement Specifications (URS) and Quality Risk Assessment for Equipment and Automated Systems (QRAES). Engage with design engineers and SMEs to clarify system intent and operational requirements. Ensure alignment with quality, automation, and engineering teams on critical parameters and documentation. Create Commissioning Test Plans that translate design intent into testable steps. Coordinate with the Automation Team to incorporate all automation functional testing. Collaborate with SMEs to ensure system requirements are accurately reflected in test plans. Develop Installation, Operational, and Qualification (IOQ) protocols. Prepare and submit summary reports documenting commissioning and qualification activities. System Ownership and Execution Take custody of the system post-construction and maintain ownership through C&Q completion. Perform Lockout/Tagout (LOTO) for system safety. Conduct pre-startup safety checks and risk assessments. Prepare daily pre-task plans and verify team readiness for safe execution. Attend daily commissioning meetings to coordinate activities. Execute commissioning and IOQ protocols. Resolve issues arising during execution. Participate in Factory Acceptance Tests (FATs) and Site Acceptance Tests (SATs) as required. Requirements: Bachelor’s degree in Engineering, Biotechnology, Life Sciences, or a related technical discipline 10+ years of role-specific experience Experience supporting CQV activities within GMP-regulated pharmaceutical or biotechnology environments Hands-on experience with CIP systems and automated cleaning processes Strong understanding of CQV lifecycle documentation (IQ/OQ/PQ protocols and reports) Ability to work independently while coordinating with cross-functional project teams Strong technical documentation and communication skills Experience using digital validation platforms such as Kneat Experience supporting FAT/SAT, commissioning, and equipment startup Familiarity with automated process systems and PLC-based equipment Ex…