Senior Software Engineer – Medical Devices (Hybrid)

Avanos Medical, Inc.; Alpharetta, Northern (GA, KY); Hybrid; USD 130,000 - 180,000; Full time

Benefits offered by this job

Benefits from day 1

Onsite gym

Onsite cafeteria

Job summary

Avanos Medical, Inc. is seeking a Senior Software Engineer for its Alpharetta, GA-based R&D team. You will review external software deliverables, maintain product documentation, and ensure traceability across software lifecycle activities for connected medical devices.

You will collaborate with Systems Engineering, Quality, Regulatory, and external CDMOs, and support design controls, V&V activities, and product knowledge transfer. This hybrid role requires onsite presence Tue–Thu.

Qualifications

• Bachelor’s degree in software engineering, Computer Engineering, or related.
• 8–10 years of architecture and software development experience.
• Ability to read embedded code and interface documentation.
• Experience with design controls and regulatory documentation.

Responsibilities

• Lead assigned product, subsystem, or component design activities through feasibility, development, verification, validation, design transfer, and commercialization.
• Interpret, review, and assess software deliverables with external partners and CDMOs.
• Develop and maintain system and software documentation including requirements, architecture, interface definitions, and traceability.
• Support requirements management and traceability across system requirements, software requirements, design outputs, risk controls, verification and validation activities.
• Read and interpret embedded software, firmware, and application-level code to support technical reviews and knowledge transfer.

Skills

Embedded software

Software architecture

Requirements management

Technical writing

Cross-functional collaboration

Code comprehension

Education

Bachelor’s degree in software engineering or related

Tools

Jama

Polarion

Arena

Job description

Avanos Medical, Inc. is seeking a Senior Software Engineer for its Alpharetta, GA-based R&D team. You will review external software deliverables, maintain product documentation, and ensure traceability across software lifecycle activities for connected medical devices.

You will collaborate with Systems Engineering, Quality, Regulatory, and external CDMOs, and support design controls, V&V activities, and product knowledge transfer. This hybrid role requires onsite presence Tue–Thu.