Onsite Engineering Lead - Pharma CQV & GMP

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. 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.