×
Register Here to Apply for Jobs or Post Jobs. X

Principal Engineer – Drug Delivery Device Development; Electro-Mechanical Combination Products

Job in New Albany, Franklin County, Ohio, 43054, USA
Listing for: 3 Key Consulting, Inc.
Full Time position
Listed on 2026-06-23
Job specializations:
  • Engineering
    Biomedical Engineer, Medical Device Industry, Quality Engineering, Product Engineer
Salary/Wage Range or Industry Benchmark: 52 - 57 USD Hourly USD 52.00 57.00 HOUR
Job Description & How to Apply Below
Position: Principal Engineer – Drug Delivery Device Development (Electro-Mechanical Combination Products)[...]

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

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

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 Principal 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

D​OE/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 of different subsystems.
  • Create and execute 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.
  • 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 Master’s degree and 5 years of experience OR Bachelor’s degree and 7 years of experience OR Associate’s 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 21

      CFR
      820
    • EU Medical Device requirements
    • Medical Electrical Equipment EN 60601
  • 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 to apply and will be considered!!!

Red Flags

Not flexible for the working shift/hours required and limitation to travel. Approximately 1-2x per month

#J-18808-Ljbffr
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)
0
200
Filters
Education Level
Experience Level (years)
Posted in last:
Salary