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Micro Medical Device Jobs (NOW HIRING)

Aerotek

Manufacturing Technician

Irvine, CA · On-site

... micro balances, and coating machines. * Skill in handling delicate medical device components and performing inspections using microscopes or magnification tools. * Strong documentation skills ...

Aerotek

Manufacturing Technician

Irvine, CA · On-site

... micro balances, and coating machines. * Skill in handling delicate medical device components and performing inspections using microscopes or magnification tools. * Strong documentation skills ...

krg technology inc

Developer with Tester

Alameda, CA

Major Skill: u Micro controllers u C Programming u White box testing u Embedded Device testing u Medical domain u Wi-Fi Additional Information All your information will be kept confidential according ...

Resolution Medical

Director of Operations

Fridley, MN · On-site

$144K - $200K/yr

... micro manufacturing, driving innovation in the medical device industry. With rapid expansion across all our locations, we continue to push the boundaries of technology while fostering a dynamic ...

RESOLUTION MEDICAL LLC

Director of Operations

Fridley, MN · On-site

$144K - $200K/yr

Description Company Overview Resonetics is a global leader in advanced engineering, prototyping, product development, and micro manufacturing, driving innovation in the medical device industry. With ...

Resonetics

Senior Manufacturing Engineer

Bethel, CT · On-site

$88K - $120K/yr

Overview Resonetics is a global leader in advanced engineering, prototyping, product development, and micro manufacturing, driving innovation in the medical device industry. With rapid expansion ...

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Micro Medical Device information

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$21

$49

$96

How much do micro medical device jobs pay per hour?

As of Jul 1, 2026, the average hourly pay for micro medical device in the United States is $49.84, according to ZipRecruiter salary data. Most workers in this role earn between $35.10 and $59.62 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Micro Medical Device Engineer, and why are they important?

To thrive as a Micro Medical Device Engineer, you need expertise in biomedical engineering, microfabrication, and materials science, often with at least a bachelor's or master's degree in a related field. Familiarity with CAD software, cleanroom processes, and relevant regulatory standards such as ISO 13485 or FDA guidelines is typical. Strong problem-solving abilities, attention to detail, and effective teamwork are essential soft skills in this role. These competencies ensure the design, development, and manufacturing of safe, reliable, and innovative micro-scale medical devices for patient care.

What are micro medical devices?

Micro medical devices are extremely small tools or implants, often at the millimeter or even micrometer scale, designed for medical applications such as diagnostics, drug delivery, or minimally invasive surgeries. These devices leverage advanced materials and miniaturized technology to perform precise functions within the body, often accessing areas that are difficult to reach with traditional devices. Examples include micro-needles, implantable sensors, and tiny surgical instruments. The development of micro medical devices has improved patient outcomes by reducing recovery times and minimizing tissue damage.

What are some common challenges faced by professionals working in micro medical device development?

Professionals in micro medical device development often encounter challenges such as adhering to strict regulatory standards, ensuring biocompatibility and safety of miniature components, and managing the complexities of integrating advanced technologies at a micro scale. Collaboration with cross-functional teams—including engineers, clinicians, and regulatory experts—is crucial to address these challenges effectively. Additionally, staying updated with rapid advancements in materials science and manufacturing techniques is essential for success in this innovative field.

What is the difference between Micro Medical Device vs Medical Device Technician?

AspectMicro Medical DeviceMedical Device Technician
Required CredentialsTypically requires a biomedical or mechanical engineering degree or certificationRequires technical training or certification in medical device repair and maintenance
Work EnvironmentResearch labs, manufacturing facilities, or quality control settingsHospitals, clinics, or repair centers
Employer & Industry UsageMedical device manufacturing companies, biotech firmsHospitals, medical equipment service companies
Common Search & Comparison IntentUnderstanding roles in medical device developmentMaintenance and repair of medical equipment

Micro Medical Device professionals focus on designing and developing tiny medical devices, often requiring engineering expertise. Medical Device Technicians primarily handle the maintenance, repair, and calibration of medical equipment used in healthcare settings. While both roles are integral to the medical device industry, they differ in responsibilities, work environments, and required credentials.

More about Micro Medical Device jobs
What cities are hiring for Micro Medical Device jobs? Cities with the most Micro Medical Device job openings:
What states have the most Micro Medical Device jobs? States with the most job openings for Micro Medical Device jobs include:
What job categories do people searching Micro Medical Device jobs look for? The top searched job categories for Micro Medical Device jobs are:
Micro Medical Device jobs near you
Infographic showing various Micro Medical Device job openings in the United States as of June 2026, with employment types broken down into 5% As Needed, 12% Full Time, 81% Part Time, 1% Temporary, and 1% Nights. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $103,662 per year, or $49.8 per hour.
Engineer Principal, Drug Delivery Medical Device Process Development - (JP14606)

Engineer Principal, Drug Delivery Medical Device Process Development - (JP14606)

3 Key Consulting

New Albany, OH

$50 - $56/hr

Other

Posted 23 days ago

Job description

Job Title:Engineer Principal, Drug Delivery Medical Device Process Development - (JP14606)
Location:New Albany, OH. 43054
Employment Type:Contract
Business Unit:Site Process development
Duration:1+ years with possible extension or conversion to FTE
Posting Date:10/10/2025
Pay Rate:$50 - $56/hour W2 with benefits
Notes:Only qualified candidates need apply. Onsite AOH - Monday - Friday - Standard 8-5. Very occasional need to have candidates work later into the day due to occasional set up that may be needed. Approximately 1-2x per month. Also, CANDIDATES MUST BE ABLE TO TRAVEL INTERNATIONALLY.
3 Key Consulting is hiring anEngineer Principal, Medical Device Process Development, for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
Our ideal candidate will have 10 years of experience. (See below for details). This position will be onsite in New Albany, OH., Monday - Friday - Standard 8-5. Very occasional need to have candidates work later into the day due to occasional set up that may be needed. Approximately 1-2x per month.
  • The qualified candidate will lead teams in the development of drug delivery devices. Scope includes a wide range of devices, such as; needle protection systems, fluid transfer devices, pen injectors, automatic pen injectors, and micro-infuser delivery pump systems.
  • The qualified candidate will lead technical teams to ensure successful device development of these mechanical and electro-mechanical medical devices.
  • The Principle Engineer will work closely with team members to develop detailed engineering specifications, device design & development, support verification, validation, and regulatory submissions of these devices.
  • The role of the Principle Engineer is to work within a cross-functional organization to utilize technologies and methodologies that support short-cycle robust device development.

Responsibilities:
  • Work cross-functionally with individuals and project teams in Marketing, Operations, and Development - Create and assess product requirements to determine technical coverage and proper integration different subsystems.
  • Create and execute to project plans and schedules
  • Develop, execute, and review architecture documents, design documents, specifications, development plans, characterization plan, verification and validation plans and other related product development documents for assigned projects.
  • Provide deep technical assistance for junior engineers.

Why is the Position Open?
Planned Project
Top Must Have Skills:
The Principle Engineer will work closely with team members to focus on the following skills:
  • Develop, execute, and design documents, specifications, development plans, characterization plan, verification and validation plans and other related product development documents for assigned projects.
  • Experience with material & test specs generation, protocol & report writing, process & test development, prototyping, design verification, DOE/SPC process optimization & validation (IQ, OQ, PQ), FMEA. - Product design/development (design control) from concept to post product launch for Europe (EMEA/CE Mark) & US (FDA/PMA/510k) submissions.
  • Strong problem solving, risk assessment, and risk management skills and capable of working on multiple projects in a deadline driven environment.
Day to Day Responsibilities:
Develop, execute, and review architecture documents, design documents, specifications, development plans, characterization plan, verification and validation plans and other related product development documents for assigned projects. In addition to troubleshoot new equipment to be implemented.
Basic Qualifications:
Doctorate degree and 3 years of experience OR Masters degree and 5 years of experience OR Bachelors degree and 7 years of experience OR Associates degree and 12 years of experience OR High school diploma / GED and 14 years of experience.
  • BS in Engineering and previous experience in a medical device industry
  • 10 years current experience with engineering processes and procedures.
  • Led projects from development through the 510k and PMA approval process.
  • Strong background in engineering and commercialization of electro-mechanical medical devices.
  • Experience with material & test specs generation, protocol & report writing, process & test development, prototyping, design verification, DOE/SPC process optimization & validation (IQ, OQ, PQ), FMEA.
  • Product design/development (design control) from concept to post product launch for Europe (EMEA/CE Mark) & US (FDA/PMA/510k) submissions.
  • Experience in drug/device combination product design and development
  • Familiar with the following standards:
    • Quality System Regulation 21CFR820
    • Risk Management ISO 14971
    • EU Medical Device requirements Council Directive 93/42/EEC
    • Medical Electrical Equipment EN 60601
  • Small scale device assembly experience.
  • Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations.
  • Strong problem solving, risk assessment, and risk management skills.
  • Must be capable of working on multiple projects in a deadline driven environment.
  • VERY IMPORTANT NOTE: Qualified candidates with either a strong Electrical Engineering, Mechanical Engineering, OR Systems/Software Engineering background need apply and will be considered.

Red Flags:
Not flexible for the working shift/hours required. Approximately 1-2x per month
Interview process:
One round panel interview
We invite qualified candidates to sendyour resume toresumes@3keyconsulting.com. Ifyou decide that you're not interested in pursuing this particular position, please feel free to take a look at the other positions on our websitewww.3keyconsulting.com/careers. You are also welcome to sharethis opportunity withanyone you think might be interested in applying for this role.

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