Nemera is a leading global manufacturer of complex drug delivery systems for the pharmaceutical industry. This role ensures compliance with applicable standards and regulatory requirements (e.g., FDA, ISO) and leads laboratory-based quality activities. The position involves hands-on experience with Test Method Validation (TMV), Design Verification (DV), and product testing. The Quality Engineer will author, execute, and review test plans, protocols, and reports to support product development, and will perform laboratory testing, data analysis, and technical investigations. Collaboration with Design Engineering, Regulatory, and Laboratory staff is essential to ensure testing activities are appropriately planned, executed, and documented. The role also supports design controls, risk management, and other quality activities as needed.
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Job Type
Full-time
Career Level
Mid Level