Software Development Process Engineer Specialist

Siemens Healthineers

Confirmed live yesterday High trust
Remote

Quick summary

Work type
Remote
Location
Remote
Salary
$109,920–$151,140 / yr
Posted
2 days ago
Freshness
Confirmed live yesterday

Market check

Salary context

Below market

How this pay compares to similar roles

Similar $171k
This role $131k
$99k most similar roles pay here $216k

This role pays less than 79% of similar roles. Most pay $137,500–$204,200 — the shaded band above. At the midpoint, this role pays about $131k versus about $171k for comparable roles.

Based on 240 similar postings.

Employer

About Siemens Healthineers

Siemens Healthineers is a leading global medical technology company, headquartered in Germany, that provides imaging, diagnostics, and artificial intelligence-driven solutions to healthcare providers.

Siemens Healthineers currently has 22 open roles on FindRole.

Listed pay typically runs $124,200–$170,775 across 22 roles with salary data.

Most-posted roles

View all roles at Siemens Healthineers

At a glance

TL;DR · Software Development Process Engineer Specialist

Software Development Process Engineer / Specialist (Medical Device) joins the PTP Processes Team to shape how software products for medical devices are developed, documented, and improved globally. This role focuses on process development, governance, and continuous improvement for software design and development lifecycle activities. The individual will author and maintain procedures, ensure compliance with regulatory standards like IEC 62304, and manage requirements, architecture, and testing concepts. Key responsibilities include partnering with global teams to align processes with Agile practices, including backlog management and user stories, while driving modernization through digitalization and AI-enabled tools. The candidate must possess a degree in Engineering or Computer Science and experience in SDLC, DevOps, and medical device software standards like SaMD. They will collaborate across functions to ensure traceability, safety, and cybersecurity for products throughout the entire lifecycle from concept to support.

What you'll do

  • Author, update, and maintain procedures and work instructions for software design and development processes.
  • Ensure software development processes comply with regulatory standards, safety requirements, and cybersecurity considerations.
  • Support organizational readiness for audits and inspections by ensuring documentation is complete and traceable.
  • Align software development lifecycle (SDLC) phases with Agile practices, including backlog management and release readiness.
  • Facilitate working sessions with global stakeholders to identify process inefficiencies and improvement opportunities.
  • Drive modernization initiatives including digitalization, artifact-driven evidence management, and AI-enabled process tools.
  • Coordinate with cross-functional teams across North America, Europe, India, and China to ensure process alignment.

What we're looking for

  • Bachelor's degree in Engineering, Computer Science, Quality, or a related field.
  • 3–10 years of experience in the medical device industry or regulated software development.
  • Experience working within Software Development Lifecycle (SDLC), Agile, or DevOps environments.
  • Understanding of design controls including requirements, V&V, and traceability.
  • Knowledge of medical device software standards such as SaMD, Digital Health IT, and IEC 62304 concepts.
  • Experience authoring procedures, work instructions, or technical documentation.
  • Ability to translate complex development practices into structured, scalable processes.
  • Export Control: “A successful candidate.

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