Intuitive Logo

Intuitive

Senior Regulatory Affairs Specialist

Posted 10 Days Ago
Be an Early Applicant
In-Office
Sunnyvale, CA
Senior level
In-Office
Sunnyvale, CA
Senior level
Leads global regulatory submissions, product registrations, and market variations for regulated medical devices. Develops regulatory strategies, advises cross-functional teams on international compliance, oversees technical files and audit documentation, manages agency communications, reviews labeling, tracks regulatory metrics, and mentors regulatory specialists.
The summary above was generated by AI
Company Description

It started with a simple idea: what if surgery could be less invasive and recovery less painful? Nearly 30 years later, that question still fuels everything we do at Intuitive. As a global leader in robotic-assisted surgery and minimally invasive care, our technologies—like the da Vinci surgical system and Ion—have transformed how care is delivered for millions of patients worldwide.

We’re a team of engineers, clinicians, and innovators united by one purpose: to make surgery smarter, safer, and more human. Every day, our work helps care teams perform with greater precision and patients recover faster, improving outcomes around the world.

The problems we solve demand creativity, rigor, and collaboration. The work is challenging, but deeply meaningful—because every improvement we make has the potential to change a life.

If you’re ready to contribute to something bigger than yourself and help transform the future of healthcare, you’ll find your purpose here.

Job Description

Primary Function of Position
This role provides expert support for regulatory project management, strategic submissions, and cross-functional compliance
activities in global regulated markets.
Essential Job Duties
• Lead global regulatory submissions for product registrations and variations.
• Develop regulatory strategies for new product development and market entry.
• Advise cross-functional teams on global compliance requirements.
• Oversee preparation of technical files and documentation for audits.
• Manage agency communications for complex product approvals.
• Provide expert guidance in interpretation of international regulations.
• Review, approve, and update regulatory labeling and documentation.
• Mentor and coach regulatory affairs specialists.
• Track and report metrics on regulatory timelines and success rates.
• Represent regulatory affairs team in project meetings.

Qualifications

Minimum 8 years of experience in regulatory affairs and bachelor’s degree in a relevant discipline, or
equivalent combination of education and experience.

Required Knowledge, Skills and Abilities
• Expertise in global regulatory requirements and registration processes.
• Advanced project leadership and communication skills.
• Technical documentation review and approval capabilities.
• Agency negotiation and strategic planning proficiency.
• Experience with audits, submissions, and training.
Physical Requirements
• Not applicable

Additional Information

Due to the nature of our business and the role, please note that Intuitive and/or your customer(s) may require that you show current proof of vaccination against certain diseases including COVID-19.  Details can vary by role.

Intuitive is an Equal Opportunity Employer. We provide equal employment opportunities to all qualified applicants and employees, and prohibit discrimination and harassment of any type, without regard to race, sex, pregnancy, sexual orientation, gender identity, national origin, color, age, religion, protected veteran or disability status, genetic information or any other status protected under federal, state, or local applicable laws.

Mandatory Notices

U.S. Export Controls Disclaimer:  In accordance with the U.S. Export Administration Regulations (15 CFR §743.13(b)), some roles at Intuitive Surgical may be subject to U.S. export controls for prospective employees
who are nationals from countries currently on embargo or sanctions status.

Certain information you provide as part of the application will be used for purposes of determining whether Intuitive Surgical will need to (i) obtain an export license from the U.S. Government on your behalf (note: the government’s licensing process can take 3 to 6+ months) or (ii) implement a Technology Control Plan (“TCP”) (note: typically adds 2 weeks to the hiring process).  

For any Intuitive role subject to export controls, final offers are contingent upon obtaining an approved export license and/or an executed TCP prior to the prospective employee’s
start date, which may or may not be flexible, and within a timeframe that does not unreasonably impede the hiring need. If applicable, candidates will be notified and instructed on any requirements for these purposes. 

We will consider for employment qualified applicants with arrest and conviction records in accordance with fair chance laws.

Preference will be given to qualified candidates who do not reside, or plan to reside, in Alabama, Arkansas, Delaware, Florida, Indiana, Iowa, Louisiana, Maryland, Mississippi, Missouri, Oklahoma, Pennsylvania, South Carolina, or Tennessee.

This position may be filled at a different job level than listed here depending on
business need and/or on the selected candidate’s experience, knowledge and skills.
Compensation will be based primarily on the job level at which the role is filled and the
candidate’s qualifications, consistent with applicable law.

We provide market-competitive compensation packages, inclusive of base pay, incentives, benefits, and equity. It would not be typical for someone to be hired at the top end of range for the role, as actual pay will be determined based on several factors, including experience, skills, and qualifications. The target compensation ranges are listed.

Similar Jobs

2 Days Ago
In-Office
Irvine, CA, USA
92K-130K Annually
Senior level
92K-130K Annually
Senior level
Healthtech • Pharmaceutical
Represent Regulatory Affairs on medical device manufacturing and product development teams. Review technical documentation, guide regulatory strategy, prepare and oversee domestic and international submissions, support agency interactions and audits, monitor global regulations, and ensure labeling and product documentation comply with applicable requirements. The role focuses on Class II and III transcatheter heart valve devices and requires extensive regulatory submission experience.
Top Skills: 510(K)Ce MarkingGudidIdeMedical Device Regulatory SubmissionsPmaStedTechnical Files
6 Days Ago
In-Office
145K-160K Annually
Senior level
145K-160K Annually
Senior level
Healthtech
Supports U.S. and international medical device regulatory submissions, including 510(k)s, registrations, and letters to file. Provides regulatory guidance across product development, biocompatibility, sterilization, packaging, labeling, clinical strategy, promotional claims, and post-market activities. Partners with Quality, R&D, Operations, Clinical, Marketing, and Legal; supports FDA interactions, audits, inspections, CAPAs, complaints, and global compliance monitoring.
Top Skills: 510(K)CapaEqmsEu MdrFdaNcmr
14 Days Ago
In-Office
116K-156K Annually
Senior level
116K-156K Annually
Senior level
Hardware • Healthtech • Manufacturing
Leads regulatory strategy and submissions for Class III medical devices across US and international markets. Evaluates product and manufacturing changes, reviews technical, labeling, risk, promotional, and quality documents, supports audits, engages regulatory bodies, maintains compliance knowledge, and improves regulatory processes. The role requires cross-functional collaboration, project timeline management, and regulatory guidance for new and existing cardiac device products.
Top Skills: FdaMedical Device Regulatory SubmissionsUs And International Medical Device Regulations

What you need to know about the Los Angeles Tech Scene

Los Angeles is a global leader in entertainment, so it’s no surprise that many of the biggest players in streaming, digital media and game development call the city home. But the city boasts plenty of non-entertainment innovation as well, with tech companies spanning verticals like AI, fintech, e-commerce and biotech. With major universities like Caltech, UCLA, USC and the nearby UC Irvine, the city has a steady supply of top-flight tech and engineering talent — not counting the graduates flocking to Los Angeles from across the world to enjoy its beaches, culture and year-round temperate climate.

Key Facts About Los Angeles Tech

  • Number of Tech Workers: 375,800; 5.5% of overall workforce (2024 CompTIA survey)
  • Major Tech Employers: Snap, Netflix, SpaceX, Disney, Google
  • Key Industries: Artificial intelligence, adtech, media, software, game development
  • Funding Landscape: $11.6 billion in venture capital funding in 2024 (Pitchbook)
  • Notable Investors: Strong Ventures, Fifth Wall, Upfront Ventures, Mucker Capital, Kittyhawk Ventures
  • Research Centers and Universities: California Institute of Technology, UCLA, University of Southern California, UC Irvine, Pepperdine, California Institute for Immunology and Immunotherapy, Center for Quantum Science and Engineering

Sign up now Access later

Create Free Account

Please log in or sign up to report this job.

Create Free Account