Engineering Site Lead

Validation & Engineering Group, Inc.; Hebron Estates (KY); On-site; USD 120,000 - 170,000; Full time

Job summary

Validation & Engineering Group, Inc. in Kentucky seeks an experienced Engineering Site Lead to manage on-site engineering activities at an FDA-regulated facility. This high-visibility role offers the chance to influence project direction and ensure compliance.

You will coordinate CQV, automation, process, and facilities teams, drive milestones, and maintain schedule while upholding GMP standards.

Qualifications

• 8+ years engineering experience in pharma/biotech/medical devices.
• Experience leading on-site projects or site teams.
• Strong knowledge of CQV and GMP environments.

Responsibilities

• Lead all onsite engineering activities and serve as primary contact.
• Coordinate cross-functional teams including CQV, automation, process, and facilities.
• Drive daily execution, track milestones, keep project on schedule.
• Identify and resolve issues to maintain progress.
• Support CQV activities and ensure GMP compliance.

Skills

Engineering leadership

CQV knowledge

GMP experience

On-site coordination

Strong communication

Tools

Automation systems familiarity

Job description

Validation & Engineering Group, Inc. a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethical standards for the following position:

Engineering Site Lead

We're looking for a hands-on Engineering Site Lead to support a fast-paced project at an FDA-regulated manufacturing facility in Kentucky. This is a high-visibility onsite engagement with strong potential to transition into a long-term role.

Description

• Lead all onsite engineering activities and serve as the primary point of contact
• Coordinate cross functional teams (CQV, automation, process, facilities)
• Drive daily execution, track milestones, and keep the project on schedule
• Identify and resolve issues quickly to maintain progress
• Support commissioning, qualification, and validation (CQV) activities
• Ensure compliance with GMP and safety standards
• Communicate updates clearly with stakeholders

Qualifications

• 8+ years of engineering experience in pharma, biotech, or medical device environments
• Proven experience in site leadership or project execution roles
• Strong knowledge of CQV and GMP environments
• Ability to work independently and lead on-site teams effectively
• Strong communication and problem-solving skills

Preferred

• Experience with manufacturing or lab equipment
• Familiarity with automation systems
• Experience in fast-paced or short-term project environments

Why This Role?

• Immediate impact in a high-visibility project
• Opportunity to take ownership on-site
• Potential to convert to a long term role based on performance and project needs

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 - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.

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.