Engineer II, Validation AVI

Work Schedule

Environmental Conditions

Job Description

Discover Impactful Work:

As part of the Thermo Fisher Scientific team youll do meaningful work that makes a positive impact on a global scale. Join colleagues who bring our Mission to life every dayenabling 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. With new lines being addedincluding auto-injector technologythis role offers hands-on experience in one of the most in-demand areas of the industry.

This is an entry-level opportunity designed for growth where youll gain valuable highly marketable experience in sterile manufacturing validation.

A Day in the Life:

This role offers a balance of technical documentation and hands-on execution:

• 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:

• Bachelors degree in Engineering Life Sciences Chemistry or related field
• 02 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 manufacturingespecially sterile/aseptic environmentsis 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 (MondayFriday standard hours)
• Strong communication and teamwork skills

Why Join Us:

• Entry point into high-demand sterile validation engineering
• Hands-on learning with experienced mentors
• Exposure to cutting-edge pharmaceutical technologies (AVI & auto-injectors)
• Clear career progression into advanced validation roles