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
