Engineer II, Validation - AVI
Thermo Fisher Scientific
Thermo Fisher Scientific seeks a Validation Engineer II to support Automatic Visual Inspection operations in sterile pharmaceutical manufacturing at the Greenville facility. This entry-level role combines technical documentation with hands-on production floor work, offering structured mentorship and exposure to expanding AVI and auto-injector validation functions.
Responsibilities
- Write validation protocols, perform data analysis, and prepare documentation and reports
- Execute validation activities on production floor alongside team members in sterile environments
- Participate in data calculations, evaluations, and summary report generation
- Work directly with commercial manufacturing equipment and Automatic Visual Inspection systems
- Interface with clients and serve as point of contact as experience develops
Requirements
- Bachelor's degree in Engineering, Life Sciences, Chemistry, or related field
- 0–2+ years validation or GMP environment experience preferred
- Strong technical writing and documentation skills
- High attention to detail and quality-focused mindset
- Pharmaceutical manufacturing or sterile/aseptic environment exposure strongly preferred
- Knowledge of cGMP and regulated environments preferred
- Familiarity with IQ/OQ/PQ concepts a plus
Vacancy posted 7 days ago
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