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Medical Device Manager Jobs in Virginia (NOW HIRING)

Novocure

Territory Manager, TGI (Virginia)

Richmond, VA · On-site

$14K - $175K/yr

Territory Manager (Thoracic/Pancreatic), Virginia Field Based / Full Time / Permanent At Novocure ... Experience selling disruptive or market-creating medical device or healthcare technology.

Novocure

Territory Manager, TGI (Virginia)

Richmond, VA · On-site

$14K - $175K/yr

Territory Manager (Thoracic/Pancreatic), Virginia Field Based / Full Time / Permanent At Novocure ... Experience selling disruptive or market-creating medical device or healthcare technology.

AAMI

Vice President - Industry

Arlington, VA

Collaborate with product development and management teams to ensure offerings meet the unique needs of medical device manufacturers and regulators. Sales and Marketing Enablement: Work closely with ...

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Medical Device Manager information

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How much do medical device manager jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for medical device manager in Virginia is $38.94, according to ZipRecruiter salary data. Most workers in this role earn between $22.44 and $52.13 per hour, depending on experience, location, and employer.

What is a medical device manager?

Medical Device Managers are professionals responsible for overseeing the development, production, and regulatory compliance of medical devices within healthcare organizations or manufacturing companies. They coordinate teams, manage product lifecycles, ensure products meet safety standards, and liaise with regulatory bodies such as the FDA. Their work helps ensure that medical devices are safe, effective, and brought to market efficiently. In addition, they may also handle budgeting, quality assurance, and post-market surveillance of devices.

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

To excel as a Medical Device Manager, you need a solid background in biomedical engineering, regulatory compliance, and product lifecycle management, often supported by a relevant degree and industry experience. Familiarity with quality management systems (such as ISO 13485), FDA or CE regulatory processes, and CRM or ERP software is typically required. Strong leadership, problem-solving, and communication skills help in guiding cross-functional teams and managing client relationships. These competencies ensure the safe, effective launch and maintenance of medical devices in a highly regulated market.

What are some common challenges faced by medical device managers in ensuring regulatory compliance?

Medical Device Managers often encounter challenges in navigating complex and evolving regulatory requirements across different regions. Ensuring that products meet the standards set by agencies like the FDA or EMA requires continuous monitoring of changes in regulations, thorough documentation, and close collaboration with regulatory affairs and quality assurance teams. Additionally, balancing compliance with timely product development and market launch can be demanding, as even minor oversights can lead to delays or costly recalls.

What is the difference between Medical Device Manager vs Medical Equipment Coordinator?

AspectMedical Device ManagerMedical Equipment Coordinator
CertificationsRegulatory and management certifications, such as RAC or PMPBasic healthcare or equipment management certifications
Work EnvironmentHealthcare facilities, manufacturing companies, regulatory agenciesHospitals, clinics, equipment suppliers
Employer & IndustryMedical device companies, hospitals, biotech firmsHospitals, clinics, medical equipment vendors
Primary FocusOverseeing device development, compliance, and lifecycle managementManaging equipment inventory, maintenance, and distribution

The Medical Device Manager primarily focuses on overseeing the development, compliance, and lifecycle of medical devices, often requiring management certifications. In contrast, the Medical Equipment Coordinator handles equipment inventory, maintenance, and distribution within healthcare settings. Both roles are essential in healthcare but differ in scope and responsibilities.

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

The most popular types of Medical Device jobs in Virginia are:

What are popular job titles related to Medical Device Manager jobs in Virginia?

For Medical Device Manager jobs in Virginia, the most frequently searched job titles are:

What job categories do people searching Medical Device Manager jobs in Virginia look for?

The top searched job categories for Medical Device Manager jobs in Virginia are:

What cities in Virginia are hiring for Medical Device Manager jobs?

Cities in Virginia with the most Medical Device Manager job openings:

Medical Device Manager jobs near you
Infographic showing various Medical Device Manager job openings in Virginia as of August 2026, with employment types broken down into 1% As Needed, 71% Full Time, 22% Part Time, and 6% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $80,985 per year, or $38.9 per hour.

Senior Staff Packaging Engineer

Addison Group

Leesburg, VA • On-site

$128K - $136K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 8 days ago

Job description

Senior Staff Packaging Engineer
Location: Leesburg, VA (5-15% Travel)
Compensation: $128,000 - $136,000 Base Salary + Performance Bonus Potential
Company Overview
Our client is a leading privately held medical device manufacturer focused on developing innovative products that improve patient outcomes. This highly collaborative engineering organization partners closely with product development, manufacturing, quality, and supply chain teams to design and validate packaging solutions that protect complex medical devices throughout manufacturing, sterilization, transportation, and clinical use.
Position Summary
The Senior Staff Packaging Engineer serves as a technical leader responsible for the design, development, validation, and continuous improvement of sterile and non-sterile medical device packaging systems. This individual will lead packaging projects from concept through commercialization while partnering with cross-functional engineering teams, suppliers, and manufacturing operations to deliver reliable, compliant, and cost-effective packaging solutions.
This role offers significant ownership over packaging strategy, design standards, testing protocols, and continuous improvement initiatives supporting new product development.
Responsibilities
  • Lead the design, development, and implementation of sterile and non-sterile medical device packaging systems from concept through production release.
  • Develop packaging design standards, engineering procedures, and best practices that optimize product protection, manufacturability, cost, and regulatory compliance.
  • Create detailed packaging designs and engineering documentation utilizing CAD software (SolidWorks or Creo preferred).
  • Develop specifications for primary, secondary, and tertiary packaging components.
  • Design, execute, and analyze packaging validation and performance testing to ensure compliance with applicable regulatory and quality standards.
  • Partner with Product Development, Manufacturing, Quality, Regulatory, and Supply Chain teams throughout new product development programs.
  • Design transportation cases, trays, and packaging systems supporting sterilization, shipment, storage, and clinical use.
  • Lead packaging-related risk assessments including DFMEA, PFMEA, and other design control documentation.
  • Collaborate with suppliers and contract manufacturers to optimize packaging designs, improve manufacturability, and reduce overall costs.
  • Identify and implement continuous improvement and value engineering opportunities while maintaining product quality and performance.
  • Stay current on emerging packaging materials, technologies, and industry best practices.

Required Qualifications
  • Bachelor's degree in Packaging Engineering, Mechanical Engineering, Materials Science, Quality Engineering, Microbiology, or a related technical discipline.
  • Minimum 6 years of experience in packaging engineering or packaging design and development.
  • Minimum 2 years of CAD design experience utilizing SolidWorks, Creo, or similar software.
  • Strong understanding of medical device packaging requirements, Quality System Regulations (QSR), and packaging validation methodologies.
  • Experience managing multiple engineering projects within a regulated manufacturing environment.
  • Strong technical communication, project management, and cross-functional leadership skills.

Preferred Experience
  • Medical device packaging design.
  • Sterile packaging systems.
  • Packaging validation and testing.
  • Transportation and distribution packaging.
  • Risk management (DFMEA/PFMEA).
  • Supplier collaboration and design for manufacturability.
  • Cost reduction and value engineering initiatives.
  • New product development within regulated manufacturing environments.

Benefits
  • Competitive base salary
  • Performance-based bonus opportunity
  • Medical, Dental & Vision Insurance
  • 401(k) with Company Match
  • Paid Time Off & Holidays
  • Paid Parental Leave
  • Professional Development & Training
  • Career Advancement Opportunities

Additional Information
  • Full-time, onsite position based in Leesburg, VA.
  • Approximately 5-15% travel required.
  • Opportunity to serve as a technical leader within a collaborative R&D organization while developing innovative packaging solutions supporting advanced medical technologies.

Compensation: $128,000 - $136,000 Base Salary + Performance Bonus Potential
• Pay for this role is competitive and based on experience, qualifications, and performance. The typical compensation range is $128,000-$136,000 annually, with eligibility for performance-based bonuses and a comprehensive benefits package. Final compensation is determined based on experience level, technical expertise, and overall market alignment.

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