6141 - Project Engineer / Project Engineer

Verista, Inc.•Indianapolis, IN

4h•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 Project Engineer Position Overview We are seeking a Project Engineer to support manufacturing and equipment modification activities within a regulated pharmaceutical environment. This role will be responsible for coordinating and executing engineering projects related to equipment relocation, testing, and validation readiness for the Insulin manufacturing line. The Project Engineer will work cross-functionally with Manufacturing, Quality, Validation, Automation, and Facilities teams to ensure projects are completed safely, compliantly, and on schedule.

Requirements

Bachelor’s degree in Engineering (Mechanical, Chemical, Electrical, Industrial, or related discipline)
2–5 years of engineering experience in a pharmaceutical, biotech, or regulated manufacturing environment
Hands-on experience supporting equipment modifications, relocations, or testing activities
Working knowledge of Change Control processes in a GMP environment
Strong ability to coordinate cross-functional activities and communicate effectively with diverse stakeholders
Strong organizational skills with attention to detail and documentation accuracy
Onsite requirement in Indianapolis, IN

Nice To Haves

Familiarity with manufacturing equipment used in sterile or insulin production environments preferred

Responsibilities

Support engineering activities related to autoclavable stopper arm implementation and offline stopper test station installation and testing
Lead and support the NVPM relocation project (Area 105B – Insulin Line), including equipment relocation, reinstallation, and functional testing
Coordinate execution of equipment modifications and process changes within GMP manufacturing areas
Author, review, and support Change Controls in accordance with site and corporate quality systems
Collaborate cross-functionally with Manufacturing, Quality Assurance, Validation, Automation, and Maintenance teams
Track project timelines, deliverables, risks, and dependencies to ensure on-time execution
Support commissioning and testing activities to ensure equipment is fit for intended use
Ensure compliance with safety, GMP, and regulatory requirements throughout project execution
Participate in project meetings, document action items, and provide clear status updates to stakeholders