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Director Medical Device Jobs (NOW HIRING)

Kellton Tech

Medical Device Assembler

Madison, WI · On-site

$23 - $24/hr

Medical device, pharmaceutical industry Competencies: Self-directed Teamwork Good communication skills Proficient with computer systems Critical thinking Decision making Quality focused ...

Kelly Services

Medical Device Assembly

Irvine, CA

$22.50/hr

Assemble medical device components using hand tools, fixtures, and specialized equipment * Follow ... Requests for accommodation related to our application process can be directed to the Kelly Human ...

New

Crown Medical, Inc.

Medical Device Rep

Sarasota, FL · On-site

$82K - $113K/yr

Medical Sales Territory Representative - Entry Level We are a leading Medical Device and Equipment ... as directed by management in order to grow market share; * Consistently develop a partnership ...

Crown Medical, Inc.

Medical Device Rep

Boca Raton, FL · On-site

$82K - $113K/yr

Medical Sales Territory Representative - Entry Level We are a leading Medical Device and Equipment ... as directed by management in order to grow market share; * Consistently develop a partnership ...

Crown Medical, Inc.

Medical Device Rep

Carlsbad, CA · On-site

$82K - $113K/yr

Medical Sales Territory Representative - Entry Level We are a leading Medical Device and Equipment ... as directed by management in order to grow market share; * Consistently develop a partnership ...

Crown Medical, Inc.

Medical Device Rep

Santa Barbara, CA · On-site

$82K - $113K/yr

Medical Sales Territory Representative - Entry Level We are a leading Medical Device and Equipment ... as directed by management in order to grow market share; * Consistently develop a partnership ...

Crown Medical, Inc.

Medical Device Rep

Albuquerque, NM · On-site

$82K - $113K/yr

Medical Sales Territory Representative - Entry Level We are a leading Medical Device and Equipment ... as directed by management in order to grow market share; * Consistently develop a partnership ...

Crown Medical, Inc.

Medical Device Rep

Austin, TX · On-site

$82K - $113K/yr

Medical Sales Territory Representative - Entry Level We are a leading Medical Device and Equipment ... as directed by management in order to grow market share; * Consistently develop a partnership ...

LivaNova, PLC

Medical Device Assembler

Arvada, CO · On-site

$19.50 - $21/hr

Medical Device Production Assembler Build Products That Help Change Lives Arvada, CO | Full-Time ... Take ownership of your work and see the direct impact of your contributions. * Be part of a culture ...

LivaNova

Medical Device Assembler

Arvada, CO · On-site

$19.50 - $21/hr

Medical Device Production Assembler Build Products That Help Change Lives Arvada, CO | Full-Time ... Take ownership of your work and see the direct impact of your contributions. * Be part of a culture ...

Crown Medical, Inc.

Medical Device Rep

Baton Rouge, LA · On-site

$82K - $113K/yr

Medical Sales Territory Representative - Entry Level We are a leading Medical Device and Equipment ... as directed by management in order to grow market share; * Consistently develop a partnership ...

SlingShot Connections

Be Seen First

Medical Device Assembler

San Clemente, CA · On-site

$22.10/hr

Work under direction from management or engineering staff with direct oversight * Other duties as ... Comfortable working in a regulated environment (medical device experience is a plus) * Ability to ...

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Director Medical Device information

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$76.5K

$177.2K

$304.5K

How much do director medical device jobs pay per year?

As of Sep 13, 2026, the average yearly pay for director medical device in the United States is $177,191.00, according to ZipRecruiter salary data. Most workers in this role earn between $136,000.00 and $203,500.00 per year, depending on experience, location, and employer.

What is a director medical device?

A Director of Medical Devices is a senior leadership role responsible for overseeing the development, regulatory compliance, and commercialization of medical devices. They manage cross-functional teams, ensuring products meet industry standards and regulatory requirements. This role often involves strategic planning, budget management, and collaboration with R&D, quality assurance, and marketing teams. Directors also play a key role in ensuring patient safety and product effectiveness while driving business growth.

What are the key skills and qualifications needed to thrive as a director medical device?

To thrive as a Director Medical Device, you need deep knowledge of medical device regulations, product development, and leadership, often supported by a degree in engineering, life sciences, or a related field. Familiarity with tools like quality management systems (QMS), regulatory submission platforms, and certifications such as PMP or Six Sigma are highly valuable. Strategic thinking, cross-functional communication, and change management are vital soft skills that help drive innovation and lead diverse teams. These competencies are essential to ensure product quality, regulatory compliance, and successful market delivery in a complex and rapidly evolving industry.

What are some of the main challenges a director medical device faces in leading product development teams?

Directors of Medical Device often encounter challenges such as managing regulatory compliance across multiple markets, ensuring seamless collaboration between cross-functional teams, and keeping projects on track amid evolving industry standards. They must also balance innovation with risk mitigation to bring new products to market safely and efficiently. Navigating these demands requires strong leadership and a deep understanding of both engineering and regulatory requirements, as well as the ability to adapt to new technologies. Overcoming these challenges is key to driving organizational success and maintaining a competitive edge within the medical device sector.

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

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Director Medical Device jobs near you
Infographic showing various Director Medical Device job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 77% Full Time, 15% Part Time, and 7% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $177,191 per year, or $85.2 per hour.

Quality Director (Medical Device / USCT)

Remote

Midjourney
Scientific Research and Development Services • 11 - 50 employees
Learn more about Midjourneyexternal

Full-time

This job post has expired 2 days ago. Applications are no longer accepted.

Job description

What you'll do
  1. Own and evolve the Quality Management System (QMS) to support a regulated medical device development program, including design controls and DHF maintenance.
  2. Establish and enforce requirements traceability: user needs → design requirements → verification/validation artifacts and change control.
  3. Define and run the program-level V&V strategy (verification, validation, and test coverage), including test plans, protocols, reports, and acceptance criteria.
  4. Drive risk management activities (e.g., DFMEA / PFMEA, hazard analyses) and ensure mitigations are reflected in requirements and verification.
  5. Lead document control: reviews, approvals, training, retention, and audit readiness.
  6. Partner with engineering to make quality "native" to the dev workflow (automated testing, release gates, software configuration management).
  7. Prepare the program for audits and inspections, including hands-on audit leadership.
What we're looking for
  • Senior experience leading quality for complex hardware + software products in a regulated environment.
  • Deep familiarity with design controls, DHF, document control, risk management, and verification planning.
  • Strong systems thinking and the ability to translate ambiguous product intent into testable requirements.
  • Comfortable collaborating directly with multidisciplinary engineering (recon/ML, embedded, mechanical, EE, cloud).
Useful experience
  • Regulated product quality leadership (ISO 13485 / 21 CFR 820 or equivalent), including audit readiness and FDA-facing work.
  • eQMS + document control fluency (e.g., Greenlight Guru) that integrates cleanly with modern engineering workflows.

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