6176 - CIP Senior Process Engineer / Senior Process Engineer

Verista, Inc.•Holly Springs, NC

3d•Onsite

About The Position

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 Position Summary: We are seeking an experienced Senior Process Engineer to support process and utility systems within a regulated biopharmaceutical manufacturing environment at our Holly Springs site. This role is fully onsite and requires strong hands-on technical expertise with Clean-In-Place (CIP) systems, process design, and supporting utilities. The Process Engineer will be responsible for the design, review, and optimization of CIP systems and associated utilities to ensure robust, compliant, and efficient manufacturing operations. The ideal candidate has deep technical knowledge of CIP system design, understands the interaction between process equipment and utilities, and can collaborate cross-functionally in a GMP environment.

Requirements

Bachelor’s degree in Chemical Engineering, Mechanical Engineering, or a related engineering discipline
Proven experience as a Process Engineer in a regulated pharmaceutical or biotechnology environment
Strong hands-on experience with Clean-In-Place (CIP) systems
Demonstrated experience in: System design reviews
Process design and documentation
Utility design and utility-system integration related to CIP
Solid understanding of GMP principles and regulated manufacturing environments
Ability to work 100% onsite in Holly Springs, NC

Nice To Haves

Experience supporting large-scale biopharmaceutical manufacturing operations
Familiarity with commissioning, qualification, and validation activities related to CIP systems
Strong communication skills and ability to work cross-functionally
Experience supporting system upgrades or new system installations

Responsibilities

Lead and support CIP system design, review, and optimization for manufacturing processes
Perform process design activities, including development and review of process flow diagrams (PFDs), piping and instrumentation diagrams (P&IDs), and system layouts
Review and assess system design documentation to ensure alignment with operational, safety, and regulatory requirements
Provide technical expertise in utilities supporting CIP systems, including water systems, steam, chemical distribution, and waste handling
Support implementation of process and utility design changes in a GMP environment
Collaborate with cross-functional teams including Manufacturing, Engineering, Validation, Quality, and Facilities
Ensure designs meet GMP, safety, and regulatory compliance standards
Participate in troubleshooting, continuous improvement initiatives, and process optimization efforts