#Senior #DevOps #Engineer | Medical Devices / FDA | Full Remote | Inglés Avanzado
Argentina · 

Nos encontramos en la búsqueda de un/a Senior DevOps Engineer para incorporarse a un equipo internacional de I+D vinculado al desarrollo de productos de Medical Devices regulados por FDA.

Buscamos un perfil altamente técnico, autónomo y con fuerte orientación al ownership, capaz de liderar mejoras en procesos DevOps, automatización y CI/CD dentro de entornos complejos y regulados.

Role Overview
Join a dynamic team as a Senior DevOps Engineer supporting FDA‑regulated medical device products. This role involves providing expert guidance on CI/CD pipelines, and workflows to development teams working on embedded software in C. You will play a key part in optimizing tools and processes, ensuring smooth and reliable product development.
Key Responsibilities

• Design, implement, and optimize CI/CD pipelines and workflows to streamline product development.
• Architect solutions to overcome technical limitations, ensuring scalable and reliable deployment processes.
• Lead migration and management of DevOps tools such as GitLab and Jenkins, including transitioning off Jenkins when necessary.
• Support embedded software development activities, particularly in C, with additional expertise in C++, Python, Linux, Bash and optionally Rust.
• Identify gaps in current processes, recommend improvements, and execute solutions to boost efficiency.
• Design and implement secure secrets management solutions for CI/CD pipelines, protecting credentials, tokens, and keys in compliance with security and regulatory requirements.
• Collaborate across multiple projects, demonstrating flexibility and adaptability to changing requirements and technologies.
• Ensure DevOps processes align with Company processes that support FDA regulations for medical device software, including security, traceability, auditability, and validation readiness.

 Required Skills & Experience:

• Proven experience with modern DevOps tools, CI/CD pipelines, and workflow automation.
• Proven experience working in a Medical Device environment in an FDA regulated environments
• Strong expertise in GitLab, Jenkins, and migration strategies.
• Proficiency in C/C++, Python,  Linux, Windows and familiarity with Rust is a plus.
• Hands-on experience with secrets management in DevOps pipelines, including secure storage, access control, rotation, and integration with CI/CD workflows.
• Skilled in troubleshooting, architecting solutions, and overcoming technical limitations.
• Ability to identify process gaps and drive improvements.

Soft Skills

• Self-motivated with a proactive approach; capable of working independently without constant supervision.
• Flexible working hours to accommodate mission-critical tasks, including occasional late hours and weekends.
• Excellent team player with strong collaboration skills, capable of engaging with stakeholders and management effectively.
• Adaptable to changing project needs and evolving technologies.

Condiciones principales:

• 15 días de PTO por año (10 días hábiles de vacaciones + 5 días adicionales) + feriados locales
• Horario alineado a Eastern Standard Time (aprox. 8 a.m. a 5 p.m.)