Engineer II, Validation - AVI

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office

Discover Impactful Work

As part of the Thermo Fisher Scientific team, you’ll do meaningful work that makes a positive impact on a global scale. Join colleagues who bring our Mission to life every day—enabling customers to make the world healthier, cleaner, and safer. Join our growing validation team supporting Automatic Visual Inspection (AVI) operations, a critical and expanding function within sterile pharmaceutical manufacturing.

A Day in the Life

• ~60% desk-based: writing validation protocols, data analysis, reporting, and documentation
• ~40% on the production floor: executing validation activities alongside team members
• Partner with experienced engineers for hands-on training and execution
• Participate in data calculations, evaluations, and summary reports
• Gradually interface with clients and become a point of contact
• Work directly with commercial manufacturing equipment in sterile/inspection environments

What to Expect

• Structured onboarding with SOP training and hands-on mentorship
• Direct exposure to AVI and sterile pharmaceutical processes
• Career growth within a rapidly expanding function (AVI + auto-injector lines)
• Collaborative team environment (team of ~4 engineers)

Keys to Success

• Education & Experience: Bachelor’s degree in Engineering, Life Sciences, Chemistry, or related field 0–2+ years of experience in validation or regulated/GMP environment preferred
• Required Skills & Experience: Strong technical writing and documentation skills High attention to detail and quality-focused mindset Comfort working around large-scale manufacturing equipment Ability to learn quickly in a hands-on environment Exposure to pharmaceutical manufacturing—especially sterile/aseptic environments—is strongly preferred and highly valued
• Additional Requirements: Knowledge of cGMP and regulated environments preferred Familiarity with IQ/OQ/PQ concepts a plus Ability to work onsite in Greenville, NC (Monday–Friday, standard hours) Strong communication and teamwork skills