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Engineer II, Validation - AVI

Greenville, North Carolina, USA💼 Full-time🗓 2026-06-29 → 2026-07-31

Core

Entry-level validation engineer supporting Automatic Visual Inspection (AVI) operations in sterile pharmaceutical manufacturing, balancing technical documentation with hands-on execution on the production floor.

Role type

Entry-level validation engineer (sterile pharmaceutical manufacturing)

Builds

Validation protocols, data analysis reports, and execution of validation activities for AVI and auto-injector lines

Domain

Sterile pharmaceutical manufacturing / Automatic Visual Inspection (AVI)

Deliverable

production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work

Required skills

Technical writing, data analysis, attention to detail, ability to work with large-scale manufacturing equipment, knowledge of cGMP and regulated environments, familiarity with IQ/OQ/PQ concepts

Preferred skills

Experience in sterile/aseptic environments, exposure to pharmaceutical manufacturing

Technologies

AVI systems, auto-injector technology

Responsibilities

Writing validation protocols, executing validation activities on the production floor, performing data calculations and evaluations, generating summary reports, interfacing with clients

Seniority

Entry-level, hands-on IC

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