Software Development Process Engineer / Specialist (Medical Device)

Siemens Healthineers

Remote

Quick summary

Work type
Remote
Location
Remote
Salary
$109,920–$151,140 / yr
Posted
3 days ago

Market check

Salary context

Below market

How this pay compares to similar roles

Similar $173k
This role $131k
$98k most similar roles pay here $222k

This role pays less than 78% of similar roles. Most pay $136,375–$209,750 — the shaded band above. At the midpoint, this role pays about $131k versus about $173k 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 27 open roles on FindRole.

Listed pay typically runs $131,910–$181,379 across 24 roles with salary data.

Most-posted roles

View all roles at Siemens Healthineers

At a glance

TL;DR · Software Development Process Engineer / Specialist (Medical Device)

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As a Process Development Specialist at Varian, a Siemens Healthineers company, you will join the PTP Processes Team as an integral member responsible for developing and governing software design and development processes. Your day-to-day tasks include authoring and maintaining procedures that ensure compliance with regulatory standards while supporting agile practices and digital transformation initiatives. You will collaborate closely with global engineering teams to facilitate process improvements and support organizational readiness for audits, leveraging your expertise in medical device software standards such as IEC 62304. The ideal candidate has a background in software development lifecycle management, experience in regulated environments, and strong technical literacy combined with excellent communication skills to drive continuous improvement across distributed teams.

Skills

Agile DevOps SDLC IEC 62304 SaMD Digital Health IT Design Controls V&V Traceability AI Process Automation Digital Transformation Documentation Regulatory Compliance Medical Device Industry Software Development Quality Assurance Requirements Management Architecture Design Testing Concepts

What you'll do

  • Author and maintain software design and development procedures aligned with regulatory standards.
  • Ensure processes support efficient and compliant software development across the product lifecycle.
  • Support process alignment with agile practices for iterative development cycles and release readiness.
  • Identify inefficiencies in software development processes and drive continuous improvement initiatives.
  • Facilitate working sessions to understand team execution and suggest process improvements.

What we're looking for

  • Bachelor’s degree in Engineering, Computer Science, Quality, or related field.
  • 3–10 years of experience in medical device industry or regulated software development.
  • Understanding of software requirements, architecture, testing concepts, and design controls.
  • Experience with medical device software standards (SaMD, Digital Health IT) and IEC 62304 concepts.
  • Ability to author procedures, work instructions, and technical documentation.
  • Strong collaboration skills for working across global, cross-functional teams.

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