Engineering Site Lead
Listed on 2026-08-21
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Engineering
Validation Engineer, Quality Engineering, Biomedical Engineer, Process Engineer
Validation & Engineering Group, Inc. (V&EG), a Pinnaql company
, is a leading services provider delivering solutions to the Pharmaceutical, Biotechnology, Medical Device, Chemical, and Food industries across Engineering, Project Management, Validation, Compliance, Laboratory, and Computer Systems.
We are seeking a talented, dedicated professional committed to the highest ethical standards for the following position:
Engineering Site LeadWe are seeking a hands-on Engineering Site Lead to provide onsite engineering leadership at an FDA-regulated manufacturing facility in Kentucky. This highly visible role will serve as the primary engineering point of contact, coordinating cross-functional teams and driving the successful execution of engineering, equipment, automation, and CQV activities.
ResponsibilitiesLead and coordinate day-to-day onsite engineering activities
Serve as the primary engineering point of contact for site stakeholders
Coordinate cross-functional teams, including CQV, Automation, Process, Facilities, Maintenance, Quality, and Operations
Drive project and engineering execution, priorities, schedules, milestones, and deliverables
Proactively identify and resolve technical, schedule, and operational issues
Support commissioning, qualification, and validation (CQV) activities for manufacturing and laboratory equipment and systems
Support equipment installation, startup, upgrades, troubleshooting, and continuous improvement initiatives
Ensure engineering activities comply with GMP, safety, quality, and site requirements
Provide clear, timely communication on project status, risks, priorities, and issues to key stakeholders
Qualifications8+ years of engineering experience within pharmaceutical, biotechnology, medical device, or other FDA-regulated manufacturing environments
Demonstrated experience leading onsite engineering activities, projects, or cross-functional technical teams
Strong knowledge of GMP and CQV requirements
Hands-on experience with manufacturing and/or laboratory equipment and systems
Experience supporting equipment installation, startup, qualification, troubleshooting, or optimization
Familiarity with industrial automation and controls systems
Strong project execution, problem-solving, and organizational skills
Ability to independently manage priorities and drive issues through resolution
Excellent communication and stakeholder management skills
Ability to work onsite in Hebron, Kentucky (greater Cincinnati area)
At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.
Excited to build something meaningful together? We look forward to hearing from you.
Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.
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