Principal Technical Curriculum Developer – SaMD Product Development & QA

We are seeking a highly experienced Principal Technical Learning Consultant to help design, build, and lead the next generation of learning programs that enable teams to develop safe, compliant, and effective medical device software.
This is not a traditional training or curriculum development role.
We are looking for someone who understands how regulated healthcare software is actually developed and can translate complex regulatory, quality, systems engineering, risk management, and product development concepts into practical, role-based learning experiences for engineers, product managers, TPMs, systems engineers, quality professionals, and development leaders.
This role will play a critical part in establishing an embedded learning function supporting more than 10,000 product development professionals across Oracle Health.
What You'll Do
Build Product Development Learning Programs
Design and deliver instructor-led, workshop-based, virtual, and self-paced learning programs supporting Oracle Health's regulated product development organizations.
Create onboarding, role-based learning paths, technical workshops, certifications, and continuous education programs.
Develop scalable learning strategies that improve competency, productivity, compliance, and execution quality.
Conduct learning needs assessments and partner with leadership to identify capability gaps and organizational priorities.
Teach Teams How to Build Regulated Medical Devices
Develop and deliver learning experiences focused on:
Software as a Medical Device (SaMD)
Medical Device Development Lifecycle
Design Controls
Requirements Engineering
Systems Engineering
Traceability Management
Risk Management
Hazard Analysis
FMEA
Fault Tree Analysis
HAZOP
Verification & Validation
Software Anomaly Management
Change Control
Technical File Creation & Maintenance
Submission Readiness
Audit Readiness
Regulatory Documentation
AI Governance and Responsible AI Development
Product Development Processes and Tooling
Partner Across Product Development
Work closely with Engineering, Product Management, Quality, Regulatory Affairs, Clinical Safety, Cybersecurity, Human Factors, TPMs, and Compliance teams.
Collaborate with subject matter experts to transform complex technical knowledge into practical learning experiences.
Support adoption of new tools, processes, standards, and methodologies across development organizations.
Build learning content that enables teams to effectively perform regulated development activities within Oracle's Quality Management System.
Support SaMD and Regulatory Excellence
Help teams understand how to operationalize and comply with:
IEC 62304 – Medical Device Software Lifecycle Processes
IEC 82304 – Healthcare Software Safety and Security
ISO 13485 – Medical Device Quality Management Systems
ISO 14971 – Risk Management for Medical Devices
IEC 62366 – Usability Engineering
IEC 81001-5-1 – Cybersecurity for Health Software
ISO/IEC 27001 – Information Security
ISO/IEC 42001 – AI Management Systems
FDA Software Guidance
EU MDR / IVDR
IMDRF SaMD Frameworks
Develop Modern Learning Solutions
Create instructor-led training, workshops, simulations, labs, job aids, videos, eLearning modules, process guides, and certification programs.
Develop case studies, real-world scenarios, and hands-on exercises that help teams apply learning directly to their day-to-day work.
Measure learning effectiveness through assessments, feedback, business outcomes, and adoption metrics.
Continuously improve learning content based on learner feedback, audit findings, process improvements, and organizational priorities.
Disclaimer:
Certain U.S. based or U.S. customer or client-facing roles may be required to comply with applicable requirements, such as immunization/occupational health mandates, and/or drug testing requirements.
Range and benefit information provided in this posting are specific to the stated locations only
US: Hiring Range in USD from: $91,400 to $187,000 per annum. May be eligible for bonus and equity.
Oracle maintains broad salary ranges for its roles in order to account for variations in knowledge, skills, experience, market conditions and locations, as well as reflect Oracle's differing products, industries and lines of business.
Candidates are typically placed into the range based on the preceding factors as well as internal peer equity.
Oracle US offers a comprehensive benefits package which includes the following:
1. Medical, dental, and vision insurance, including expert medical opinion
2. Short term disability and long term disability
3. Life insurance and AD&D
4. Supplemental life insurance (Employee/Spouse/Child)
5. Health care and dependent care Flexible Spending Accounts
6. Pre-tax commuter and parking benefits
7. 401(k) Savings and Investment Plan with company match
8. Paid time off: Flexible Vacation is provided to all eligible employees assigned to a salaried (non-overtime eligible) position. Accrued Vacation is provided to all other employees eligible for vacation benefits. For employees working at least 35 hours per week, the vacation accrual rate is 13 days annually for the first three years of employment and 18 days annually for subsequent years of employment. Vacation accrual is prorated for employees working between 20 and 34 hours per week. Employees working fewer than 20 hours per week are not eligible for vacation.
9. 11 paid holidays
10. Paid sick leave: 72 hours of paid sick leave upon date of hire. Refreshes each calendar year. Unused balance will carry over each year up to a maximum cap of 112 hours.
11. Paid parental leave
12. Adoption assistance
13. Employee Stock Purchase Plan
14. Financial planning and group legal
15. Voluntary benefits including auto, homeowner and pet insurance
The role will generally accept applications for at least three calendar days from the posting date or as long as the job remains posted.
Career Level - IC4
Required 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, product development, technical program management, or technical learning.
Experience working in regulated industries, preferably healthcare, medical device, or Software as a Medical Device (SaMD) environments.
Strong understanding of software development lifecycle processes.
Direct experience with one or more of the following:
Requirements engineering
Risk management
Hazard analysis
Traceability
Verification and validation
Technical documentation
Design controls
Quality systems