This role pays less than
91%
of similar roles. Most pay
$174,600–$246,700
— the shaded band above.
At the midpoint, this role pays about
$139k
versus about
$211k
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.
Principal Technical Curriculum Developer – SaMD Product Development & QA serves as a key member of the Oracle Health team, where you will design, build, and lead advanced learning programs for professionals developing regulated medical device software. You will create instructor-led workshops, virtual training, and self-paced modules focused on Software as a Medical Device (SaMD) development lifecycles, risk management, hazard analysis, and traceability. The role requires translating complex regulatory requirements into practical experiences for engineers, product managers, and quality professionals. You will utilize core competencies in systems engineering, requirement engineering, and verification and validation while ensuring compliance with standards such as IEC 62304, ISO 13485, and FDA guidelines. Your work addresses the critical challenge of operationalizing safety, cybersecurity, and regulatory requirements within cloud-native healthcare software environments to ensure products are safe, compliant, and effective for clinical use.
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.
Develop educational content covering SaMD lifecycle, design controls, traceability, hazard analysis, and AI governance.
Collaborate with subject matter experts to transform technical knowledge into scalable learning strategies and tools.
Create diverse learning assets including simulations, labs, job aids, videos, and certification modules.
Measure training effectiveness through assessments, feedback, and adoption metrics to continuously improve content.
Teach teams how to operationalize compliance standards such as IEC 62304, ISO 13485, and FDA guidelines.
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 such as healthcare, medical devices, or Software as a Medical Device (SaMD) environments.
Strong understanding of software development lifecycle processes.
Direct experience with requirements engineering, risk management, hazard analysis, traceability, verification and validation, technical documentation, design controls, or quality systems.
Exceptional communication, facilitation, and presentation skills to influence highly technical audiences across multiple organizations.
Proficiency in instructional design methodologies and adult learning principles.