Top 3 principal program manager Jobs in orlando, fl

Principal Specialist, Regulatory Science
Stryker —Orlando, FL
- $102,600 - $238,400 a year
- Full-time
- Hybrid work
- Master's degree
- Bachelor's degree
- Doctor of Philosophy
- Health savings account
- AD&D insurance
2d
Principal
Richard Milburn Academy —Kissimmee, FL
- Full-time
- School experience
- Classroom
- High school
Quick Apply

More jobs to discover

Find similar jobs that you might be interested in.

Dean of Students & Campus Operations
UCP of Central Florida —Orlando, FL
Oversee daily front office operations to ensure a welcoming, efficient, and well-organized environment for students, families, and visitors.
$52,000 - $55,000 a year
Quick Apply
7d
Preschool Director
Ladybird Academy of Avalon Park —Orlando, FL
Spot check that follow-up phone calls have been made to prospective tours as needed. Organize field trips and other activities such as Picture Day, Fundraisers,…
$55,000 - $60,000 a year
Quick Apply

Show more similar jobs

Explore jobs in cities nearby

Check out jobs in cities near your current location, Columbus

Principal — K–8 Charter School
Adkins & Company —Columbus, OH
Master’s degree in Educational Leadership, Administration, or a closely related field required; additional curriculum leadership coursework preferred.
Up to $90,000 a year
Quick Apply
Assistant Principal 7-12
Arts and College Preparatory Academy —Columbus, OH
Assistant Principal will support the Testing Coordinator in overseeing the planning, training, security, and administration of state-mandated and standardized…
$87,500 a year

Show more jobs in cities nearby

I want to receive the latest job alert for principal program manager in orlando, fl

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

principal program manager jobs near orlando, fl

Regulatory Specialist jobs in Orlando, FL

Regulatory Specialist jobs in Carol Stream, Il

Regulatory Specialist jobs in Rocky River, Oh

Regulatory Specialist jobs in Hackensack, Nj

Document Specialist jobs in North Carolina

Regulatory Writer jobs in Remote

Regulatory Specialist jobs in New York, Ny

School Principal jobs in Saratoga County, Ny

Assistant Principal jobs in Peoria, Az

School Principal jobs in South Carolina

School Assistant Principal jobs in Tucson, Az

Assistant Principal jobs in Baltimore, Md

Wyoming Principal jobs in Wyoming

Assistant Principal jobs in Austin, Tx

School Principal jobs in Oklahoma

Principal Specialist, Regulatory Science

Stryker -
Orlando, FL

Apply Now

Job Details

Full-time
$102,600 - $238,400 a year
2 days ago

Benefits

Health savings account
AD&D insurance
Employee stock purchase plan
Paid holidays
Disability insurance
Health insurance
Dental insurance
401(k)
Flexible spending account
Vision insurance
Prescription drug insurance

Qualifications

Medical device testing
ISO standards
Bachelor's degree
Sterile processing regulatory compliance
Biomedical regulatory compliance
Clinical quality assurance standards
Validation design

Full Job Description

Why join Stryker?

Looking for a place that values your unique talents? Discover Stryker's award-winning culture.
We are proud to offer you our total rewards package which includes bonuses, healthcare, insurance benefits, retirement programs, wellness programs, as well as service and performance awards – not to mention various social and recreational activities, all of which are location specific.

Job description

We are excited to be named one of the World’s Best Workplaces by Fortune Magazine! We are proud to offer you 12 paid holidays annually. For an overview of our benefits and time off, please follow this link to learn more:US Stryker employee benefits.

Stryker is seeking a Principal Specialist, Regulatory/Clinical Science (Biocompatibility & Sterility) for our Orthopedic Technologies Division | Mako & Enabling Technologies. This is a remote position based in the Eastern Time Zone.

As the Principal Specialist, Regulatory Science, you will provide both strategic direction and hands-on technical leadership in biocompatibility and sterility, ensuring consistent, compliant, and scalable practices across product development and sustaining activities. You will operate as a senior individual contributor driving alignment, standards, and execution across the business.

What You Will Do

Define and implement Clinical Sciences strategies for biocompatibility and sterility across new product development and sustaining programs
Lead development of quality system frameworks, standards, and processes to support compliant clinical science practices
Own and deliver clinical sciences work products, including test strategies, risk assessments, and regulatory documentation
Provide technical leadership on biocompatibility evaluations (ISO 10993), sterilization validation (e.g., EO, radiation), and microbiological risk
Integrate clinical science strategies with risk management and design controls to ensure alignment across product lifecycle stages
Identify and implement process improvements, standardization, and tools to enhance efficiency, reduce rework, and improve quality outcomes
Partner with cross-functional teams to influence program decisions, resolve technical challenges, and maintain execution timelines
Mentor team members and contribute to building scalable capabilities through development of best practices and technical frameworks

What You Need

Required

Bachelor’s degree in Biomedical Engineering, Biology, Microbiology, Materials Science, or related field
Minimum 10 years of experience in the medical device industry with focus on biocompatibility and/or sterility
Demonstrated expertise in ISO 10993 biocompatibility standards and sterilization validation methods
Experience applying ISO 14971 risk management principles within product development

Preferred

Advanced degree (Master’s or PhD) in a related scientific discipline
Experience supporting orthopedic, robotic, or implantable medical device products
Experience supporting regulatory submissions, audits, or inspections
Experience developing or scaling technical functions, frameworks, or processes

Posted Date: 06/03/2026
This role will be posted for a minimum of 3 days.

United States of America Pay Ranges:

Puerto Rico: $102,600 - $171,000 USD Annual
USN: $110,100 - $183,400 USD Annual
US5: $115,600 - $192,600 USD Annual
US10: $121,100 - $201,700 USD Annual
US15: $126,600 - $210,900 USD Annual
US20: $132,100 - $220,100 USD Annual
US30: $143,100 - $238,400 USD Annual

View the U.S. work location and transparency guide to find the pay range for your location.

Health benefits include: Medical and prescription drug insurance, dental insurance, vision insurance, critical illness insurance, accident insurance, hospital indemnity insurance, personalized healthcare support, wellbeing program and tobacco cessation program. Financial benefits include: Health Savings Account (HSA), Flexible Spending Accounts (FSAs), 401(k) plan, Employee Stock Purchase Plan (ESPP), basic life and AD&D insurance, and short-term disability insurance. Stryker offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually. Depending on customer requirements employees and new hires in sales and field roles that require access to customer accounts as a function of the job may be required to obtain various vaccinations as an essential function of their role.

Apply Now

Refine Your Search

principal program manager jobs in orlando, fl

Principal Specialist, Regulatory Science

Principal

More jobs to discover

Explore jobs in cities nearby

I want to receive the latest job alert for principal program manager in orlando, fl

Explore jobs in more locations

Why join Stryker?

Job description

Job Seeker Tools

Employer Tools

Browse

Stay Connected