Associate Engineer, Quality Systems & AWS

NoxPharm; North Chicago (IL); Presencial; USD 90.000 - 130.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Paid time off

Health/dental/vision insurance

401(k)

Descripción de la vacante

AbbVie is seeking a data and software specialist to independently perform analyses and implement solutions under supervision. You will work with modern programming languages, cloud deployments, and regulatory requirements to support global operations.

Responsibilities include analyzing results, troubleshooting software, updating documentation, and contributing to project time/cost estimates while ensuring compliance with GxP, FDA, and ISO standards.

Formación

• Bachelor's degree with 2+ years in software development lifecycle including git, CI/CD, testing.
• Experience with C#, Java or Python/Node.js and .NET frameworks.
• Knowledge of GxP, FDA, ISO 9001 and regulatory technology practices.

Responsabilidades

• Perform routine tasks competently and independently and generate reliable results.
• Analyze and critique results, noting significant variances or deviations.
• Troubleshoot algorithms, protocols, and software programs.
• Modify protocols to suit changing business needs and learn new methods.
• Obtain estimates from vendors and input into project time and cost estimates.
• Produce and maintain technical documentation for work products.
• Ensure adherence to corporate policies including data security and SDLC.
• Leverage AWS expertise to architect high-performance, cost-optimized global solutions.

Conocimientos

Git

CI/CD

Testing

C#

Java

Python/Node.js

.NET Frameworks

GxP Compliance

Regulatory Tech

Educación

Bachelor's Degree

Herramientas

.AWS

Descripción del empleo

AbbVie is seeking a data and software specialist to independently perform analyses and implement solutions under supervision. You will work with modern programming languages, cloud deployments, and regulatory requirements to support global operations.

Responsibilities include analyzing results, troubleshooting software, updating documentation, and contributing to project time/cost estimates while ensuring compliance with GxP, FDA, and ISO standards.