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Vp Medical Device Jobs (NOW HIRING)

VP Trade Compliance

Peachtree Corners, GA · On-site

$119K - $159K/yr

Regulatory and Medical Device Compliance: ensure compliance with trade regulations as they apply to finished goods, capital equipment, service parts, digital health components, clinical trial ...

Instylla, Inc. is a privately held medical device company based in Bedford, MA, focused on ... The Vice President of Operations is primarily responsible for production, manufacturing engineering ...

Vice President of Operations

Bedford, MA · On-site

$200K - $260K/yr

Instylla, Inc. is a privately held medical device company based in Bedford, MA, focused on ... The Vice President of Operations is primarily responsible for production, manufacturing engineering ...

... medical device companies, and medical societies collect, analyze, and act on patient-reported ... ABOUT THE ROLE PatientIQ is searching for its next VP of Marketing - a pipeline-obsessed ...

Real Chemistry is seeking a Vice President or Senior Vice President, Medical Strategy. Title and level will be determined based on the candidate's experience, leadership scope, and alignment with ...

The Vice President of Medical Affairs is a member of the senior executive team that has oversight of medical care provided in the institution. The VPMA works closely with the senior nursing executive ...

The Vice President Regulatory Affairs & Quality will be an experienced professional with a track record of success in the medical device industry. The responsibilities of this position are, but are ...

As Vice President, Medical Strategy, this leader serves as a strategic scientific partner for pharmaceutical and life sciences clients, helping shape brand strategy, medical communications, and ...

Job Title:Vice President, Medical and Health Sciences Advancement Department:Advancement | Development Vice President Position Overview Ohio State is seeking a talented leader to elevate the ...

VP, Operations

Bethel, CT · On-site

$225K - $300K/yr

The Vice President of Operations is a key leader responsible for driving operational excellence in ... Join Resonetics and be part of a team that's redefining medical device manufacturing. If you're ...

VP, Operations

Bethel, CT · On-site

$225K - $300K/yr

The Vice President of Operations is a key leader responsible for driving operational excellence in ... Join Resonetics and be part of a team that's redefining medical device manufacturing. If you're ...

Showing results 41-60

Vp Medical Device information

See salary details

$43.5K

$157.5K

$277.5K

How much do vp medical device jobs pay per year?

As of Sep 2, 2026, the average yearly pay for vp medical device in the United States is $157,532.00, according to ZipRecruiter salary data. Most workers in this role earn between $115,000.00 and $190,000.00 per year, depending on experience, location, and employer.

What does a VP Medical Device do?

A VP of Medical Device is a senior executive responsible for overseeing the strategy, development, and commercialization of medical device products within a company. They lead teams in research and development, ensure regulatory compliance, and manage relationships with key stakeholders such as healthcare providers and regulatory bodies. Their role is crucial in guiding the company’s product portfolio, driving innovation, and ensuring that medical devices meet market needs and safety standards. They also play a pivotal role in setting business goals, managing budgets, and ensuring overall profitability of the medical device division.

What are some common challenges faced by a VP Medical Device in balancing regulatory compliance with innovation?

A VP of Medical Device often faces the challenge of ensuring that new product developments comply with strict regulatory requirements while still fostering innovation and speed to market. Balancing thorough documentation, quality assurance, and adherence to FDA or international standards can slow down the innovation process. However, successful VPs work closely with cross-functional teams—such as R&D, regulatory affairs, and quality assurance—to create processes that support both compliance and creative problem-solving. Building strong relationships with regulatory agencies and staying updated on evolving guidelines also helps streamline approvals and facilitate smoother product launches.

What are the key skills and qualifications needed to thrive as a VP Medical Device, and why are they important?

To thrive as a VP Medical Device, you need in-depth knowledge of medical device regulations, product development, and business strategy, usually supported by an advanced degree in engineering, life sciences, or business. Familiarity with FDA/CE regulatory processes, quality management systems (e.g., ISO 13485), and industry-standard project management tools is essential. Strong leadership, negotiation, and cross-functional communication skills enable effective team management and stakeholder engagement. These qualities are crucial for ensuring product compliance, driving innovation, and achieving commercial success in a highly regulated industry.

What is the difference between Vp Medical Device vs Product Manager Medical Device?

AspectVp Medical DeviceProduct Manager Medical Device
CredentialsTypically requires engineering, business, or healthcare-related degrees; experience in medical device industrySimilar credentials; often with engineering, marketing, or healthcare backgrounds
Work EnvironmentExecutive leadership, strategic planning, cross-departmental collaborationProduct development, market research, cross-functional teams
Employer & Industry UsageMedical device companies, healthcare organizationsMedical device companies, healthcare technology firms
Search & Comparison IntentHigh overlap in industry, strategic role, and credentialsRelated role focusing on product lifecycle and market success

The Vp Medical Device typically holds a senior leadership role overseeing company strategy and operations, while the Product Manager Medical Device focuses on managing specific products throughout their lifecycle. Both roles require industry experience and relevant credentials, but the Vp has broader strategic responsibilities compared to the product-focused role of the Product Manager.

More about Vp Medical Device jobs

What cities are hiring for Vp Medical Device jobs?

Cities with the most Vp Medical Device job openings:

What are the most commonly searched types of Medical Device jobs?

The most popular types of Medical Device jobs are:

What states have the most Vp Medical Device jobs?

States with the most job openings for Vp Medical Device jobs include:

Infographic showing various Vp Medical Device job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution, with an average salary of $157,532 per year, or $75.7 per hour.

VP Trade Compliance

Intuitive Surgical

Peachtree Corners, GA

$119K - $159K/yr

Full-time

Posted 21 days ago


Intuitive Surgical rating

8.7

Company rating: 8.7 out of 10

Based on 18 frontline employees who took The Breakroom Quiz


Job description

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
The Vice President of Trade Compliance reports to the SVP Planning and Logistics and is
responsible for establishing, governing and enforcing Intuitive’s global trade compliance
framework for medical devices, instruments, accessories, capital equipment, service parts,
software, and indirect materials. The role ensures full legal compliance with all applicable import,
export, customs, sanctions, and trade regulations while supporting uninterrupted patient care,
regulatory approvals and global commercial operations. The position balances regulatory rigor
with operational continuity in a highly regulated environment where delays and enforcement
actions may impact healthcare delivery.
Essential Job Duties

Continue to build and lead a global trade compliance
organization. Establish training programs tailored to
manufacturing, service, commercial teams, distributors,
logistics providers, and customs brokerage. Direct
responsibility for compliance with inbound materials,
manufacturing cross border transactions, and finished goods into markets. Ensure
escalation, issue management, and document controls.
• Serve as primary interface with customs and export control authorities, health authorities
and trade regulators. Represent the company in industry groups addressing medical
device trade issues. Manage relationships with brokers, consultants, outside counsel,
and regulatory advisors.
• Oversee trade compliance systems integrated with ERP, WMS, TMS, and Global Trade
Management platforms. UDI, lot, serial, and device history record data. Ensure accuracy
of HS codes, ECCNs, valuation, and origin and the sku and serialized device level. Drive
automation to reduce clearance delays and improve audit readiness

Qualifications

Required Skills and Experience

Strategic Leadership: define and own the trade compliance strategy across R&D,
manufacturing, service, and commercial distribution. Proactively advise executive
leadership on trade risks affecting business continuity, and service programs. Assess
geopolitical, sanctions, and regulatory developments impacting medical device supply
chains.
• Regulatory and Medical Device Compliance: ensure compliance with trade regulations as
they apply to finished goods, capital equipment, service parts, digital health components,
clinical trial materials, samples, etc. Partner with Regulatory Affairs and Quality to ensure
trade compliance does not compromise regulatory approvals, UDI requirements, or
product traceability. Understanding FDA regulated products and global equivalents (EU
MDR, UKCA, PMDA, NMPA, ANVISA, etc.)

Governance, Policy, and Risk Management: establish and
maintain global policies covering: HS classification,
Valuation, ECCN determinations, Country-Of-Origins and
substantial transformation analysis, Free Trade Agreements
and preferential duty programs, sanctioned and denied
party screenings for institutions and distributors. Lead government audits, inquiries, and
inspections related to customs and export controls. Oversee voluntary disclosures and
corrective actions in coordination with Legal, Outside Counsel, and Quality.
• Continuity of Care: embed compliance into workflows including global manufacturing,
field service and logistics, repair networks, consignment, loaner, and emergency
replacement programs. Ensure compliant execution of bonded movement, bonded
warehouses, Free Trade Zones, and duty deferral programs. Enable tariff-mitigation
strategies without risking regulatory violations or product holds.
• Track Record: history of zero material trade violations, on time clearance of critical device
and service parts, successful audits with customs, effective tariff and duty optimization,
and institution of systems and networks

Required Education and Training 
• Proven leadership at Vice President and Director levels of global and regional
compliance teams. Demonstrated experience supporting regulated medical device or life
science supply chains.
• BS in Law, International Trade, Business, Supply Chain / Logistics, or related field
• 15+ years of experience in global trade compliance, customs, or export controls
• Trade or Custom Certifications (LCB, CCS, CUSECI, or equivalent)

Preferred Skills and Experience 
• Advanced degree
• Experience with FDA regulated products and global health authorities
• Medical device regulatory fluency and risk management. Capital equipment, software
enabled devices, serialization, service intensive portfolios

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.

Base Salary Range Region 1:$280,000 - $420,000
Base Salary Range Region 2: $280,000 - $420,000
Shift: Day
Workplace Type: Purposeful Onsite - This job requires being onsite for leader-defined events and activities which could be monthly/annually. Onsite frequency may increase based on business need.


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