×
Register Here to Apply for Jobs or Post Jobs. X

Director, Software Architecture & Engineering

Job in Center Valley, Lehigh County, Pennsylvania, 18034, USA
Listing for: Olympus Corporation
Full Time position
Listed on 2026-10-14
Job specializations:
  • Software Development
    Software Architect, Software Project Mgr/ Lead
Salary/Wage Range or Industry Benchmark: 144541 - 216812 USD Yearly USD 144541.00 216812.00 YEAR
Job Description & How to Apply Below
Location: Center Valley

Job Overview

We are seeking a Director of Software Architecture and Engineering to lead the architecture and engineering strategy for medical devices, connected health platforms, and regulated healthcare technologies. The role is headquartered in Center Valley, PA, and offers a hybrid work arrangement nationwide.

Key Responsibilities
  • Technology Strategy & Architecture Vision:
    • Define and lead long‑term architecture strategy for medical devices and connected health platforms.
    • Drive innovation in SaMD, embedded systems, IoT‑enabled devices, and cloud integration.
    • Align engineering strategy with product roadmaps, regulatory requirements, and commercialization goals.
    • Evaluate emerging technologies in digital health, remote monitoring, AI/ML diagnostics, and edge computing.
  • Medical Device Software Architecture:
    • Oversee architecture for cloud‑connected device platforms and supporting mobile and web applications.
    • Ensure interoperability with HL7, FHIR, DICOM where applicable.
    • Establish secure device‑to‑cloud communication architectures.
    • Define cybersecurity‑by‑design frameworks aligned with FDA and global guidance.
  • Regulatory & Compliance Leadership:
    • Ensure compliance with FDA 21 CFR Part 820/Part 11, ISO 13485, IEC 62304, ISO 14971, GDPR/HIPAA where applicable.
    • Oversee Design Controls, Verification & Validation and documentation processes.
    • Lead software risk management and hazard analysis activities.
    • Support regulatory submissions (510(k), CE marking, etc.) from a software perspective.
  • Engineering Execution & Quality:
    • Lead cross‑functional engineering teams including software, firmware, systems, Dev Ops, QA.
    • Implement secure software development lifecycle (SSDLC) practices.
    • Establish CI/CD pipelines suitable for regulated environments.
    • Drive system reliability, performance, and traceability across the product lifecycle.
    • Oversee technical documentation and audit readiness.
  • Organizational Leadership & Talent Development:
    • Build and scale high‑performing engineering and architecture teams.
    • Mentor engineering leaders and principal architects.
    • Establish engineering KPIs aligned with product quality and compliance.
    • Foster a culture of accountability, innovation, and regulatory excellence.
  • Executive & Cross‑Functional

    Collaboration:

    • Partner with Regulatory Affairs, Quality, Clinical, Product, and Manufacturing teams.
    • Translate technical architecture into regulatory and business impact for executives.
    • Participate in customer, auditor, and regulatory agency engagements.
    • Support M&A technical due diligence when applicable.
Required Qualifications
  • Bachelor’s or Master’s degree in Computer Science, Software Engineering, Biomedical Engineering, Electrical Engineering, or related field.
  • 12–15 years of progressive software engineering experience, with 5+ years in senior leadership roles in medical devices or regulated healthcare technology.
  • Deep expertise in IEC 62304‑compliant software development.
  • Experience with connected medical devices and cloud architecture (AWS, Azure, or GCP).
  • Strong understanding of regulatory audits and submissions.
  • Proven experience leading multidisciplinary engineering teams.
Preferred Qualifications
  • Experience with Software as a Medical Device (SaMD).
  • Familiarity with AI/ML in regulated healthcare products.
  • Experience with cybersecurity standards (FDA guidance, NIST).
  • Knowledge of interoperability standards (HL7, FHIR, DICOM).
  • Cloud or medical device quality certifications.
  • Experience in global regulatory environments (FDA, EU MDR, Health Canada, etc.).
Benefits & Compensation
  • Competitive salary range $144,541–$216,812 per year with potential for annual bonus.
  • 401(k) with company match.
  • Comprehensive medical, dental, vision coverage effective on start date.
  • 24/7 Employee Assistance Program.
  • Free live and on‑demand Wellbeing Programs.
  • Generous paid vacation, sick time, parental leave, and adoption assistance.
  • 12 paid holidays.
  • On‑site child daycare, café, fitness center (where applicable).
EEO & Accommodation Statement

Olympus is an equal‑employment opportunity employer. We are committed to providing reasonable accommodations for applicants with disabilities. Please contact  or call 1‑888‑659‑6787 for assistance.

To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)
0
200
Filters
Education Level
Experience Level (years)
Posted in last:
Salary