Executive Director Medical Device information
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$40.5K - $54.2K
7% of jobs
$72.9K is the 25th percentile. Wages below this are outliers.
$68K - $81.7K
19% of jobs
The median wage is $91.4K / yr.
$81.7K - $95.4K
18% of jobs
$95.4K - $109.1K
17% of jobs
$112.9K is the 75th percentile. Wages above this are outliers.
$109.1K - $122.9K
10% of jobs
$122.9K - $136.6K
4% of jobs
$136.6K - $150.3K
5% of jobs
$150.3K - $164K
4% of jobs
$164K - $177.8K
2% of jobs
$177.8K - $191.5K
2% of jobs
How much do executive director medical device jobs pay per year?
As of Sep 5, 2026, the average yearly pay for executive director medical device in the United States is $103,760.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,000.00 and $121,000.00 per year, depending on experience, location, and employer.
Executive Directors in the medical device industry are senior leaders responsible for overseeing the strategic direction, operational management, and regulatory compliance of a company's medical device division or organization. They guide teams in research, development, manufacturing, and marketing of medical devices while ensuring alignment with industry standards and company goals. Executive Directors also serve as key decision-makers, liaise with stakeholders, and ensure products meet safety and efficacy requirements. Their role is critical for driving innovation and maintaining a competitive edge in the market.
To thrive as an Executive Director in Medical Devices, you need extensive leadership experience, a background in life sciences or engineering, and a strong understanding of regulatory compliance, typically supported by an advanced degree. Familiarity with quality management systems (e.g., ISO 13485), FDA regulations, and enterprise resource planning (ERP) tools is essential. Exceptional strategic thinking, communication, and stakeholder management skills set top performers apart. These competencies are crucial for ensuring regulatory compliance, driving innovation, and achieving business growth in a highly regulated and competitive industry.
Executive Directors in the medical device sector often face challenges such as navigating complex regulatory requirements, ensuring cross-functional alignment among R&D, marketing, and compliance teams, and keeping pace with rapid technological advancements. Successfully addressing these challenges involves fostering transparent communication, building strong regulatory and quality assurance partnerships, and promoting continuous professional development within the team. Additionally, staying engaged with industry trends and regulatory updates can help anticipate changes and maintain a competitive edge.
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