How Much Does a Medical Device Assembly make?
Medical Device Assembly made a median salary around $45,501 in December, 2024.
The best-paid 25 percent made $53,192 probably that year, while the lowest-paid 25 percent made around $39,634.
Salary ranges can vary widely depending on many important factors, including education, certifications, additional skills, the number of years you have spent in your profession.
With more online, real-time compensation data than any other website, Salary.com helps you determine your exact pay target.
Best-Paying States for Medical Device Assembly
The states and districts that pay Medical Device Assembly the highest salary are District of Columbia (around $53,365)
, California (around $52,885)
, New Jersey (around $52,550)
, Alaska (around $52,214)
, and Massachusetts (around $52,166)
.
Frequently Asked Questions for Medical Device Assembly
Q:
What is the salary range of Medical Device Assembly in Davenport, IA?
A:
In 2024
, the lowest-paid Medical Device Assembly in Davenport, IA earned an average annual salary of $39,634
, while the highest-paid made $53,192.
Q:
What is the salary for a Medical Device Assembly in California?
A:
Medical Device Assembly employed in California earned an average salary of $52,885 in 2024.
Relevant Jobs of Medical Device Assembly
Medical Device Engineering Supervisor designs, develops, and enhances medical devices, equipment, or components to meet technical and functional specifications and standards. Utilizes CAD software and other design and modeling tools to evaluate design feasibility and communicate conceptual designs and specifications to stakeholders. Being a Medical Device Engineering Supervisor oversees prototype testing to evaluate medical device performance, reliability, and safety and collects and analyzes data for improvements. Implements mechanical and electrical engineering principles to analyze and troubleshoot malfunctions, identify root causes, and develop solutions. Additionally, Medical Device Engineering Supervisor researches and selects appropriate materials and processes to ensure product quality, performance, and manufacturability. Implements operational policies and guidelines to ensure products meet regulatory, safety, and quality requirements and standards. Develops modifications or fabrications to resolve production or assembly issues. Requires a bachelor's degree. Typically reports to a manager. The Medical Device Engineering Supervisor supervises a group of primarily para-professional level staffs. May also be a level above a supervisor within high volume administrative/production environments. Makes day-to-day decisions within or for a group/small department. Has some authority for personnel actions. To be a Medical Device Engineering Supervisor typically requires 3-5 years experience in the related area as an individual contributor. Thorough knowledge of functional area and department processes.
Medical Device Engineer I designs, develops, and enhances medical devices, equipment, or components to meet technical and functional specifications and standards. Utilizes CAD software and other design and modeling tools to evaluate design feasibility and communicate conceptual designs and specifications to stakeholders. Being a Medical Device Engineer I conducts prototype testing to evaluate medical device performance, reliability, and safety and collects and analyzes data for improvements. Utilizes mechanical and electrical engineering principles to analyze and troubleshoot malfunctions, identify root causes, and develop solutions. Additionally, Medical Device Engineer I identifies appropriate materials and processes to ensure product quality, performance, and manufacturability. Follows operational policies and guidelines to ensure products meet regulatory, safety, and quality requirements and standards. Develops modifications or fabrications to resolve production or assembly issues. Requires a bachelor's degree. Typically reports to a manager. The Medical Device Engineer I work is closely managed. Works on projects/matters of limited complexity in a support role. To be a Medical Device Engineer I typically requires 0-2 years of related experience.
Medical Device Engineer II designs, develops, and enhances medical devices, equipment, or components to meet technical and functional specifications and standards. Utilizes CAD software and other design and modeling tools to evaluate design feasibility and communicate conceptual designs and specifications to stakeholders. Being a Medical Device Engineer II conducts prototype testing to evaluate medical device performance, reliability, and safety and collects and analyzes data for improvements. Utilizes mechanical and electrical engineering principles to analyze and troubleshoot malfunctions, identify root causes, and develop solutions. Additionally, Medical Device Engineer II identifies appropriate materials and processes to ensure product quality, performance, and manufacturability. Follows operational policies and guidelines to ensure products meet regulatory, safety, and quality requirements and standards. Develops modifications or fabrications to resolve production or assembly issues. Requires a bachelor's degree. Typically reports to a manager. The Medical Device Engineer II occasionally directed in several aspects of the work. Gaining exposure to some of the complex tasks within the job function. To be a Medical Device Engineer II typically requires 2-4 years of related experience.
Medical Device Engineer III designs, develops, and enhances medical devices, equipment, or components to meet technical and functional specifications and standards. Utilizes CAD software and other design and modeling tools to evaluate design feasibility and communicate conceptual designs and specifications to stakeholders. Being a Medical Device Engineer III conducts prototype testing to evaluate medical device performance, reliability, and safety and collects and analyzes data for improvements. Utilizes mechanical and electrical engineering principles to analyze and troubleshoot malfunctions, identify root causes, and develop solutions. Additionally, Medical Device Engineer III identifies appropriate materials and processes to ensure product quality, performance, and manufacturability. Follows operational policies and guidelines to ensure products meet regulatory, safety, and quality requirements and standards. Develops modifications or fabrications to resolve production or assembly issues. Requires a bachelor's degree. Typically reports to a manager. The Medical Device Engineer III work is generally independent and collaborative in nature. Contributes to moderately complex aspects of a project. To be a Medical Device Engineer III typically requires 4-7 years of related experience.
Medical Device Engineer IV designs, develops, and enhances medical devices, equipment, or components to meet technical and functional specifications and standards. Utilizes CAD software and other design and modeling tools to evaluate design feasibility and communicate conceptual designs and specifications to stakeholders. Being a Medical Device Engineer IV conducts prototype testing to evaluate medical device performance, reliability, and safety and collects and analyzes data for improvements. Utilizes mechanical and electrical engineering principles to analyze and troubleshoot malfunctions, identify root causes, and develop solutions. Additionally, Medical Device Engineer IV identifies appropriate materials and processes to ensure product quality, performance, and manufacturability. Follows operational policies and guidelines to ensure products meet regulatory, safety, and quality requirements and standards. Develops modifications or fabrications to resolve production or assembly issues. Requires a bachelor's degree. Typically reports to a manager. The Medical Device Engineer IV work is highly independent. May assume a team lead role for the work group. A specialist on complex technical and business matters. To be a Medical Device Engineer IV typically requires 7+ years of related experience.