Senior Director Medical Device information
See salary details
$39.5K - $61.3K
3% of jobs
$61.3K - $83.1K
5% of jobs
$101.2K is the 25th percentile. Wages below this are outliers.
$83.1K - $105K
20% of jobs
$105K - $126.8K
20% of jobs
The median wage is $128.6K / yr.
$126.8K - $148.6K
19% of jobs
$159.1K is the 75th percentile. Wages above this are outliers.
$148.6K - $170.4K
16% of jobs
$170.4K - $192.2K
6% of jobs
$192.2K - $214K
5% of jobs
$214K - $235.9K
2% of jobs
$235.9K - $257.7K
2% of jobs
$257.7K - $279.5K
1% of jobs
How much do senior director medical device jobs pay per year?
As of Aug 18, 2026, the average yearly pay for senior director medical device in the United States is $142,920.00, according to ZipRecruiter salary data. Most workers in this role earn between $101,500.00 and $161,000.00 per year, depending on experience, location, and employer.
A Senior Director in Medical Device leads and manages teams responsible for the development, regulatory approval, and commercialization of medical devices. They oversee product strategy, ensure compliance with industry regulations, and collaborate with cross-functional teams such as R&D, marketing, and quality assurance. Their role also involves setting department goals, managing budgets, and building relationships with key stakeholders to drive business growth.
As a Senior Director in Medical Device, you will regularly collaborate with diverse teams such as R&D, regulatory affairs, quality assurance, marketing, and manufacturing. Your role involves facilitating communication between departments to ensure product development aligns with both regulatory standards and market needs. You’ll often lead cross-functional meetings, set project priorities, and resolve bottlenecks to keep projects on track. This collaborative environment is crucial for successfully bringing innovative medical devices to market while meeting strict compliance and quality requirements.
To thrive as a Senior Director in Medical Devices, you need extensive experience in product development, regulatory compliance, and a strong background in life sciences or engineering, often supported by an advanced degree. Familiarity with FDA regulations, ISO standards, quality management systems, and project management tools is typically required. Leadership, strategic thinking, and excellent communication are essential soft skills for guiding cross-functional teams and driving innovation. These skills ensure the safe, compliant, and successful delivery of medical devices in a highly regulated and competitive industry.
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