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Biomedical Engineer Manager Jobs in Silver Spring, MD

Castalia Systems

Biomedical Engineer Senior

Reston, VA · On-site

$108K - $149K/yr

Job Summary: Castalia Systems is seeking a Biomedical Engineer, Senior to support to the ... Must be able to demonstrate in-depth analysis of analytic operations and knowledge management ...

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Biomedical Engineer Manager information

See Silver Spring, MD salary details

$40.3K

$93.3K

$137.7K

How much do biomedical engineer manager jobs pay per year?

As of Jun 16, 2026, the average yearly pay for biomedical engineer manager in Silver Spring, MD is $93,279.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,300.00 and $114,100.00 per year, depending on experience, location, and employer.

What does a Biomedical Engineer Manager do?

A Biomedical Engineer Manager oversees the design, development, and maintenance of medical equipment and healthcare technology. They lead teams of biomedical engineers, ensuring compliance with industry regulations and safety standards. Their responsibilities include project management, budgeting, vendor coordination, and collaboration with healthcare professionals to improve medical device performance. Additionally, they may conduct research to innovate new technologies and optimize existing systems. Effective communication and leadership skills are essential for managing both technical and organizational aspects of the role.

What are the typical daily responsibilities of a Biomedical Engineer Manager?

A Biomedical Engineer Manager’s day often involves overseeing engineering teams, guiding medical device development projects, and ensuring product compliance with healthcare regulations. They regularly coordinate with cross-functional groups, including research scientists, clinicians, and regulatory specialists, to align project objectives and timelines. Managers also allocate resources, address technical and personnel challenges, and provide mentoring to junior engineers. This role requires balancing hands-on technical work with strategic planning to deliver safe, effective medical solutions on time and within budget.

What are the key skills and qualifications needed to thrive in the Biomedical Engineer Manager position, and why are they important?

To thrive as a Biomedical Engineer Manager, you need a strong background in biomedical engineering, project management experience, and often a relevant bachelor's or master's degree. Familiarity with regulatory compliance systems (such as FDA standards), medical device development tools, and quality assurance certifications like PMP or Six Sigma is highly valued. Outstanding interpersonal communication, leadership, and problem-solving skills help distinguish top performers in this role. These skills ensure successful project delivery, regulatory compliance, and effective team leadership in a complex, multidisciplinary environment.

What are the most commonly searched types of Biomedical Engineer jobs in Silver Spring, MD? The most popular types of Biomedical Engineer jobs in Silver Spring, MD are:
What are popular job titles related to Biomedical Engineer Manager jobs in Silver Spring, MD? For Biomedical Engineer Manager jobs in Silver Spring, MD, the most frequently searched job titles are:
What job categories do people searching Biomedical Engineer Manager jobs in Silver Spring, MD look for? The top searched job categories for Biomedical Engineer Manager jobs in Silver Spring, MD are:
What cities near Silver Spring, MD are hiring for Biomedical Engineer Manager jobs? Cities near Silver Spring, MD with the most Biomedical Engineer Manager job openings:
Biomedical Engineer Manager jobs near you
Senior Biomedical Engineer

Senior Biomedical Engineer

Novel Microdevices

Baltimore, MD • On-site

$100K - $140K/yr

Full-time

Posted 17 days ago

Job description

Job Title: Sr Biomedical Engineer with Electrical and firmware background
Location: 101 W Dickman St, Suite 300, Baltimore, MD 21230
Employment Type: Full-time
About Novel Microdevices:
Novel Microdevices is redefining point-of-care diagnostics with cutting-edge diagnostics products designed for rapid, reliable, and actionable medical insights. Our team is building next-generation diagnostic platforms using embedded systems, real-time image processing, and cloud-integrated data solutions to empower healthcare professionals worldwide.
Job Summary:
We are looking for a highly motivated and detail-oriented Engineer to lead testing and verification efforts for the Novel Dx device.
In this role, you will operate at the interface of Systems Engineering and assay performance, developing calibration protocols for manufacturing and driving Clinical Verification and Validation (V&V) activities. You will design and execute test strategies to ensure the device consistently meets performance and regulatory requirements.
Key Responsibilities:
  • Design Control & Regulatory Documentation
    • Maintain and organize Design History Files (DHF) in compliance with FDA 21 CFR 820 and applicable standards for 510(k) submissions
    • Develop and manage a comprehensive requirements traceability matrix (RTM) spanning user needs, product requirements, and subsystem specifications
    • Author and execute Verification & Validation (V&V) plans, protocols, and reports
    • Perform and document risk management activities including hazard analysis, FMEA, and risk mitigation strategies (per ISO 14971)
    • Lead and facilitate cross-functional design reviews, ensuring design control compliance
    • Support Corrective and Preventive Actions (CAPA) investigations and documentation arising from V&V activities

  • System Verification, Testing & Experimental Design
    • Design and execute experimental strategies to evaluate performance of engineering and biological subsystems
    • Define clear acceptance criteria aligned with product requirements and intended use
    • Develop detailed test protocols, test cases, and verification procedures with strong traceability to requirements
    • Conduct experiments, ensuring accurate data collection, logging, and traceability in compliance with quality standards
    • Analyze test data and document results in technical reports, including conclusions and recommendations
    • Collaborate with cross-functional teams to review test strategies and results

  • Calibration, Manufacturing Transfer & Process Development
    • Develop and validate calibration procedures for instruments and subsystems
    • Ensure calibration processes are robust, repeatable, and transferable to manufacturing technicians
    • Define and document acceptance/rejection criteria for instruments and subassemblies
    • Provide training and documentation to support manufacturing and quality teams
    • Support design transfer activities, ensuring smooth transition from development to production

Required Qualifications:
  • Background in biomedical, systems, or electrical/mechanical engineering which translates into cross functional ability to work with electronics/firmware and able to understand biological systems to run assays on a microfluidic device and interpret the data
  • 3+ years of relevant industry experience working with Medical Devices (IVD preferred)
  • Familiarity with FDA design controls, ISO 13485, and risk management standards
  • Strong systems thinking and communication skills to work across hardware, software, and biological interfaces

Compensation and Benefits:
  • Annual salary: Based on experience, it will be between $100,000 to $140,000 (subject to standard withholdings and deductions).
  • Bi-weekly pay schedule.
  • Eligible for the Company's Employee Stock Option Incentive Plan.
  • Access to standard benefits package including healthcare and other company-offered plans.

Additional Information:
  • Employment is at-will.
  • Role is in-person and due to the nature of the work, it cannot be supported adequately from a remote location
  • Must be authorized to work in the United States.

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