Solid understanding of how to analyze regulatory intelligence and translate it into clear implications for product development, clinical strategy, submissions, and lifecycle management. * Help ...
Solid understanding of how to analyze regulatory intelligence and translate it into clear implications for product development, clinical strategy, submissions, and lifecycle management. * Help ...
Solid understanding of how to analyze regulatory intelligence and translate it into clear implications for product development, clinical strategy, submissions, and lifecycle management. * Help ...
Solid understanding of how to analyze regulatory intelligence and translate it into clear implications for product development, clinical strategy, submissions, and lifecycle management. * Help ...
Regulatory Intelligence Specialist
$110K - $139K/yr
Solid understanding of how to analyze regulatory intelligence and translate it into clear implications for product development, clinical strategy, submissions, and lifecycle management. * Help ...
Regulatory Intelligence Specialist
$110K - $139K/yr
Solid understanding of how to analyze regulatory intelligence and translate it into clear implications for product development, clinical strategy, submissions, and lifecycle management. * Help ...
OR · On-site
As a Regulatory Intelligence Senior Consultant, you will serve as a key strategic partner to clients, delivering timely, highquality regulatory intelligence that supports informed development ...
As a Regulatory Intelligence Senior Consultant, you will serve as a key strategic partner to clients, delivering timely, high-quality regulatory intelligence that supports informed development ...
As a Regulatory Intelligence Senior Consultant, you will serve as a key strategic partner to clients, delivering timely, high-quality regulatory intelligence that supports informed development ...
The Opportunity This position serves as the Structural Heart (SH) Regulatory Affairs (RA) Global Regulatory Compliance process lead; collaborates cross-functionally as needed and keeps SH RA informed ...
The Opportunity This position serves as the Structural Heart (SH) Regulatory Affairs (RA) Global Regulatory Compliance process lead; collaborates cross-functionally as needed and keeps SH RA informed ...
The role partners closely with Global Regulatory Intelligence & Surveillance functions, RDQ leadership, Quality System Owners, Regulatory Affairs, and other cross-functional stakeholders to ensure ...
The role partners closely with Global Regulatory Intelligence & Surveillance functions, RDQ leadership, Quality System Owners, Regulatory Affairs, and other cross-functional stakeholders to ensure ...
Senior Director, Head of US Regulatory Affairs Policy & Intelligence
Washington, DC · On-site
$169K - $223K/yr
The Head of US Regulatory Policy & Intelligence is responsible for defining and executing Teva's US regulatory policy and intelligence strategy to enable timely patient access to medicines and ...
Senior Director, Head of US Regulatory Affairs Policy & Intelligence
Washington, DC · On-site
$169K - $223K/yr
The Head of US Regulatory Policy & Intelligence is responsible for defining and executing Teva's US regulatory policy and intelligence strategy to enable timely patient access to medicines and ...
The role partners closely with Global Regulatory Intelligence & Surveillance functions, RDQ leadership, Quality System Owners, Regulatory Affairs, and other cross-functional stakeholders to ensure ...
The role partners closely with Global Regulatory Intelligence & Surveillance functions, RDQ leadership, Quality System Owners, Regulatory Affairs, and other cross-functional stakeholders to ensure ...
Perform regulatory product submissions for projects covering multiple product linesas needed. Assistteam in IFUCompetitiveAnalysis and ReviewProjects asneeded ReviewClinicaldocumentsandliteraturefor ...
Perform regulatory product submissions for projects covering multiple product linesas needed. Assistteam in IFUCompetitiveAnalysis and ReviewProjects asneeded ReviewClinicaldocumentsandliteraturefor ...
Perform regulatory product submissions for projects covering multiple product linesas needed. Assistteam in IFUCompetitiveAnalysis and ReviewProjects asneeded ReviewClinicaldocumentsandliteraturefor ...
Perform regulatory product submissions for projects covering multiple product linesas needed. Assistteam in IFUCompetitiveAnalysis and ReviewProjects asneeded ReviewClinicaldocumentsandliteraturefor ...
WHAT YOU'LL DO Global Regulatory Operations is seeking aRegulatory Affairs Intelligence Specialistto join our team in St. Paul, MN. This position is focused on new and changing regulations that ...
WHAT YOU'LL DO Global Regulatory Operations is seeking aRegulatory Affairs Intelligence Specialistto join our team in St. Paul, MN. This position is focused on new and changing regulations that ...
WHAT YOU'LL DO Global Regulatory Operations is seeking aRegulatory Affairs Intelligence Specialistto join our team in St. Paul, MN. This position is focused on new and changing regulations that ...
WHAT YOU'LL DO Global Regulatory Operations is seeking aRegulatory Affairs Intelligence Specialistto join our team in St. Paul, MN. This position is focused on new and changing regulations that ...
WHAT YOU'LL DO Global Regulatory Operations is seeking a Regulatory Affairs Intelligence Specialist to join our team in St. Paul, MN. This position is focused on new and changing regulations that ...
WHAT YOU'LL DO Global Regulatory Operations is seeking a Regulatory Affairs Intelligence Specialist to join our team in St. Paul, MN. This position is focused on new and changing regulations that ...
Work withing the Stage Gate process to ensure regulatory intelligence is embedded directly into product, supply chain, and customer-facing processes. Key Accountabilities / Expected Results * Ensure ...
Work withing the Stage Gate process to ensure regulatory intelligence is embedded directly into product, supply chain, and customer-facing processes. Key Accountabilities / Expected Results * Ensure ...
Work withing the Stage Gate process to ensure regulatory intelligence is embedded directly into product, supply chain, and customerfacing processes. Key Accountabilities / Expected Results * Ensure ...
Work withing the Stage Gate process to ensure regulatory intelligence is embedded directly into product, supply chain, and customerfacing processes. Key Accountabilities / Expected Results * Ensure ...
Manager, Product Stewardship & Regulatory Affairs
$100K - $140K/yr
Work withing the Stage Gate process to ensure regulatory intelligence is embedded directly into product, supply chain, and customer‑facing processes. Key Accountabilities / Expected Results
Manager, Product Stewardship & Regulatory Affairs
$100K - $140K/yr
Work withing the Stage Gate process to ensure regulatory intelligence is embedded directly into product, supply chain, and customer‑facing processes. Key Accountabilities / Expected Results
Regulatory Fellow
Boston, MA · Hybrid
$76K - $107K/yr
... intelligence and guidance information to continuously support regulatory strategy in assigned region Informs regulatory affairs senior management on the status of regulatory strategies and tactics ...
Regulatory Fellow
Boston, MA · Hybrid
$76K - $107K/yr
... intelligence and guidance information to continuously support regulatory strategy in assigned region Informs regulatory affairs senior management on the status of regulatory strategies and tactics ...
CMC Director, Regulatory Affairs
Gaithersburg, MD · Remote
$153K - $202K/yr
... intelligence). This position reports to the Head of Regulatory Affairs. Essential Functions : * Responsible for high-quality CMC regulatory submissions in support of approval of global marketing and ...
Quick apply
CMC Director, Regulatory Affairs
Gaithersburg, MD · Remote
$153K - $202K/yr
... intelligence). This position reports to the Head of Regulatory Affairs. Essential Functions : * Responsible for high-quality CMC regulatory submissions in support of approval of global marketing and ...
Regulatory Affairs Manager
$145K - $165K/yr
Expand knowledge by analyzing current regulatory issues, guidance, initiatives and effectively communicate regulatory intelligence internally. * Contribute to the development and review of standard ...
Regulatory Affairs Manager
$145K - $165K/yr
Expand knowledge by analyzing current regulatory issues, guidance, initiatives and effectively communicate regulatory intelligence internally. * Contribute to the development and review of standard ...
Regulatory Intelligence information
See salary details
$18.99 - $26.66
19% of jobs
$26.66 - $34.33
3% of jobs
$35.90 is the 25th percentile. Wages below this are outliers.
$34.33 - $42
12% of jobs
The median wage is $46.45 / hr.
$42 - $49.67
27% of jobs
$53.04 is the 75th percentile. Wages above this are outliers.
$49.67 - $57.34
31% of jobs
$57.34 - $65.01
1% of jobs
$65.01 - $72.68
3% of jobs
$72.68 - $80.35
2% of jobs
$80.35 - $88.02
1% of jobs
$88.02 - $95.69
0% of jobs
$95.69 - $103.37
0% of jobs
$18
$50
$103
How much do regulatory intelligence jobs pay per hour?
What is a Regulatory Intelligence job?
A Regulatory Intelligence job involves monitoring, analyzing, and interpreting global regulatory developments to ensure compliance and strategic decision-making within an organization. Professionals in this role track regulatory changes, assess their impact on business operations, and provide insights to teams such as regulatory affairs, compliance, and product development. They also engage with regulatory agencies, industry groups, and databases to stay informed about evolving compliance requirements. This role is critical in highly regulated industries like pharmaceuticals, medical devices, finance, and energy.
What are the key skills and qualifications needed to thrive in the Regulatory Intelligence position, and why are they important?
To thrive in Regulatory Intelligence, you need a strong background in regulatory affairs, analytical skills, and the ability to synthesize and interpret complex regulations, typically supported by a degree in life sciences, law, or a related field. Familiarity with regulatory databases (such as Cortellis or PharmaPendium), monitoring tools, and compliance management systems is often required, alongside relevant certifications like RAC (Regulatory Affairs Certification). Excellent communication, critical thinking, and attention to detail are vital soft skills, allowing you to translate regulatory changes into actionable business guidance. These capabilities enable professionals to proactively manage compliance risks, support strategic decision-making, and maintain a competitive edge in highly regulated industries.
What are the typical daily responsibilities of a Regulatory Intelligence professional?
Regulatory Intelligence professionals are responsible for monitoring and analyzing global regulatory changes, assessing their impact on ongoing and future business activities, and synthesizing their findings into clear reports and recommendations for stakeholders. A typical day often includes scanning regulatory agency updates, interpreting new guidelines, collaborating with cross-functional teams in regulatory affairs, clinical, and legal departments, and contributing to strategic planning initiatives. You may also be tasked with developing internal alerts, maintaining compliance tracking systems, and supporting product development teams with up-to-date regulatory insights. This role is both analytical and collaborative, requiring you to proactively communicate emerging risks or opportunities to keep your organization compliant and informed.
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- Regulatory Intelligence Pharmacovigilance
- Quality Regulatory
- Vice President Hippo
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Job 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.
Primary Function of Position
Responsible for the collection, coordination, and summary of global regulatory intelligence that pertains to the company and our portfolio. Manage internal intelligence communications and act as SME for RI database; collaborate with global partners to coordinate and collect updates from their specific regions.
Essential Job Duties
- Solid understanding of how to analyze regulatory intelligence and translate it into clear implications for product development, clinical strategy, submissions, and lifecycle management.
- Help establish and refine internal regulatory intelligence processes and best practices.
- Evaluate and implement tools, databases, or systems that enhance regulatory intelligence capabilities.
- Contribute to continuous improvement of Reg Intel processes.
- Develop internal communications, training materials, and presentations to keep teams informed of relevant intelligence updates.
- Assist RI Leader in building a culture of regulatory awareness across the organization.
Required Experience and Education
- Minimum 5 years of experience in regulatory affairs and bachelor's degree in a relevant discipline, or equivalent combination of
- education and experience.
- Demonstrated ability to interpret complex regulatory information and translate it into business impact.
Required Knowledge, Skills and Abilities
- Project management abilities.
- Strong written and verbal communication.
- Project coordination and time management skills.
- Strong analytical and problem-solving skills.
- Ability to interpret and translate complex topics into simple language without losing context.
- Competence with document management systems and Microsoft Office.
Preferred Knowledge, Skills and Abilities
- Experience supporting innovative technologies such as surgical robotics, digital health, or complex medical devices.
- Familiarity with global regulatory pathways and evolving regulatory frameworks.
Physical Requirements
- Not applicable
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:Â Â 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 employeeswho 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). Â
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'sstart 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.Â
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.