This role pays less than
90%
of similar roles. Most pay
$165,000–$225,000
— the shaded band above.
At the midpoint, this role pays about
$139k
versus about
$195k
for comparable roles.
Based on 239 similar postings.
Employer
About Oracle
Oracle Corporation is a leading multinational technology company specializing in database software, cloud computing, and enterprise software.
Oracle currently has
781 open roles
on FindRole.
Listed pay typically runs
$102,300–$209,500
across 713 roles with salary data.
The Principal Technical Learning Consultant – SaMD Product Development & QA joins the Oracle Health team to design, build, and lead comprehensive learning programs for developing safe, compliant medical device software. This role involves creating instructor-led workshops, virtual training, and self-paced modules focused on Software as a Medical Device (SaMD) development lifecycles, risk management, requirements engineering, and audit readiness. The individual will translate complex regulatory concepts into practical experiences for engineers, product managers, and quality professionals. Key technical areas include IEC 62304, ISO 13485, ISO 14971, and AI governance. The role addresses the challenge of operationalizing safety, cybersecurity, and regulatory requirements within cloud-native environments. Candidates must possess expertise in hazard analysis, traceability management, and verification and validation to help teams navigate the complexities of regulated healthcare technology and medical device quality systems.
Design and deliver instructor-led workshops, virtual training, and self-paced learning programs for regulated medical device software development.
Create role-based learning paths, certifications, and onboarding programs for engineers, product managers, and quality professionals.
Translate complex regulatory requirements, risk management, and systems engineering concepts into practical, hands-on training experiences.
Teach technical teams how to perform hazard analysis, traceability management, and verification and validation activities.
Develop educational content focused on SaMD compliance, including IEC 62304, ISO 13485, and AI governance standards.
Create diverse learning materials such as simulations, labs, job aids, and videos to support internal tool adoption.
Conduct learning needs assessments to identify capability gaps and align training with organizational priorities.
Measure and improve learning effectiveness through assessments, feedback, and business outcome metrics.
What we're looking for
Bachelor's degree in Engineering, Computer Science, Healthcare Technology, Regulatory Affairs, Quality, Education, Instructional Design, or a related field.
8+ years of experience in medical device software, healthcare technology, quality engineering, systems engineering, regulatory affairs, product development, technical program management, or technical learning.
Experience working in regulated industries, specifically healthcare, medical device, or Software as a Medical Device (SaMD) environments.
Strong understanding of software development lifecycle processes and experience with requirements engineering, risk management, hazard analysis, traceability, verification, validation, design controls, and quality systems.
Exceptional communication, facilitation, and presentation skills to influence highly technical audiences across multiple organizations.
Experience with healthcare regulations and standards including IEC 62304, IEC 82304, ISO 13485, ISO 14971, IEC 62366, IEC 81001-5-1, or related standards.
Experience building and maintaining Design History Files, Technical Files, risk management files, or regulatory evidence packages for submissions and audits.
Agile
AI Tools
Automation
Roadmap Development
Scientific Informatics
laboratory, automation
Information Technology
Business Analysis
Project Management Methodology
Research and Development