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Contract Medical Device Design Jobs Near Me

Varsity Tutors

Biomedical Engineering Tutor

Columbus, OH · Remote

$18 - $40/hr

... medical device design principles while preparing students for biomedical engineering coursework ... Varsity Tutors does not contract in: Alaska, California, Colorado, Delaware, Hawaii, Maine, New ...

ICU Medical

Engineer III, Sustaining

Dublin, OH · On-site

$88K - $108K/yr

... medical device manufacturing. * Follow applicable procedures, work instructions, and regulatory requirements governing design changes and sustaining engineering activities. * Participate in ...

ICU Medical

Engineer III, Sustaining

Dublin, OH

$88K - $108K/yr

... medical device manufacturing. * Follow applicable procedures, work instructions, and regulatory requirements governing design changes and sustaining engineering activities. * Participate in ...

Socket.dev

Engineer III, Sustaining

Dublin, OH · On-site

$90 - $130/hr

... medical device manufacturing. * Follow applicable procedures, work instructions, and regulatory requirements governing design changes and sustaining engineering activities. * Participate in ...

Akraya Inc.

Device Engineer

New Albany, OH · On-site

$30 - $33/hr

... , CAD/Solidworks (intermediate) Contract Type: W2 Contract Duration: 12+ Months Location: New ... Experience in regulated industries, preferably biopharma, biomedical, or medical devices, is ...

ICU Medical

Packaging Engineer III

Dublin, OH · On-site

... design control processes, good engineering and documentation practices. The key responsibility of this position is to exercise medical device packaging subject matter expertise, sound judgement, and ...

ICU Medical

Packaging Engineer III

Dublin, OH

... design control processes, good engineering and documentation practices. The key responsibility of this position is to exercise medical device packaging subject matter expertise, sound judgement, and ...

IntelliGuard

Sr. Front End Developer

Columbus, OH · On-site

$111K - $145K/yr

... medical device regulations, security standards, and industry best practices. * Works closely with regulatory teams to ensure proper documentation. * Collaborates with UX/UI designers to design ...

Tuta Healthcare Pty Ltd.

Packaging Engineer III

Dublin, OH · On-site

$85 - $110/hr

... design control processes, good engineering and documentation practices. The key responsibility of this position is to exercise medical device packaging subject matter expertise, sound judgement, and ...

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Contract Medical Device Design information

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How much do contract medical device design jobs pay per hour?

As of Aug 30, 2026, the average hourly pay for contract medical device design 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.

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Contract Medical Device Design jobs near you
A map of the United States highlighting the number of Contract Medical Device Design job openings by state according to ZipRecruiter. The image is accompanied by a detailed chart listing the number of Contract Medical Device Design job openings in each state, with California having the most at 2 and Hawaii the least at 0.

Principal Engineer - Drug Delivery Device Development (Electro-Mechanical Combination Products) - (J

3 Key Consulting

New Albany, OH

$52 - $57/hr

Full-time

Re-posted 16 days ago

Job description

Job Title: Principal Engineer – Drug Delivery Device Development (Electro-Mechanical Combination Products) - (JP15480)
Location: New Albany, OH. 43054
Employment Type: Contract
Business Unit: Site Process Development
Duration: 1+ year (with likely extensions and/or conversion to permanent)
Posting Date: 06/15/26
Pay Rate: $52 - $57/hour W2
Notes: Only qualified candidates need apply. Onsite AOH - Monday - Friday - Standard 8-5
3 Key Consulting is hiring a Principal Engineer – Drug Delivery Device Development (Electro-Mechanical Combination Products) for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
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. International travel may be required for this position.
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
  • 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. They 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.
Why is the Position Open?
Planned Project
Top Must Have Skills:
Material & test specs generation, protocol & report writing.
Process & test development, prototyping, design verification.
DOE/SPC process optimization & validation (IQ, OQ, PQ), FMEA.
Nice to have: packaging process experience
Day to Day Responsibilities:
Position involves support of Senior Staff on initiation, design, and delivery of projects, particularly for Packaging Equipment C&Q, Characterization and Validation. Employ basic engineering skills and practices to gather user requirements and translate them into technical documentation for execution by third party firms.
 
  • 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.

Basic Qualifications:
  • BS in Engineering and previous experience in a medical device industry.
  • 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
  • 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 and limitation to travel. Approximately 1-2x per month
Unable to travel internationally
Interview process:
One round panel interview
We invite qualified candidates to send your resume to resumes@3keyconsulting.com.  If you decide that you’re not interested in pursuing this particular position, please feel free to take a look at the other positions on our website www.3keyconsulting.com/careers. You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.