Principal SaMD Learning Architect for Regulated Dev

Oracle

Olympia (WA)

On-site

USD 91,000 - 187,000

Full time

14 days+

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Job summary

Oracle Health seeks a Principal Technical Learning Consultant to design, build, and lead learning programs for regulated medical device software. You will translate complex regulatory and quality concepts into practical, role-based training for engineers, TPMs, and product leaders.

Lead onboarding, certifications, and continuous education while partnering with cross-functional teams to improve competency, compliance, and execution quality across 10,000+ product development professionals.

Qualifications

  • Bachelor’s degree in Engineering, Computer Science, Healthcare Technology, Regulatory Affairs, Quality, Education, Instructional Design, or related field.
  • 8 years of experience in medical device software, healthcare technology, quality engineering, systems engineering, regulatory affairs, or technical learning.
  • Experience in regulated industries, preferably healthcare or SaMD.
  • Strong understanding of software development lifecycle processes.
  • Direct experience with requirements engineering, risk management, hazard analysis, traceability, verification & validation, and design controls.

Responsibilities

  • Design and deliver instructor-led, workshop-based, virtual, and self-paced learning programs for regulated product development.
  • Teach learning experiences on SaMD, lifecycle processes, and regulatory documentation.
  • Collaborate with Engineering, Product Management, Quality, Regulatory Affairs, and Compliance to transform complex concepts into practical training.
  • Measure learning effectiveness and iterate content based on feedback and audits.

Skills

Learning design
Regulatory knowledge
Workshop facilitation
Stakeholder collaboration
Technical communication

Education

Bachelor’s degree in Engineering/CS/Healthcare Tech

Job description

Oracle Health seeks a Principal Technical Learning Consultant to design, build, and lead learning programs for regulated medical device software. You will translate complex regulatory and quality concepts into practical, role-based training for engineers, TPMs, and product leaders.

Lead onboarding, certifications, and continuous education while partnering with cross-functional teams to improve competency, compliance, and execution quality across 10,000+ product development professionals.

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