Principal Engineer – Drug Delivery Device Development; Electro-Mechanical Combination Products
Listed on 2026-06-23
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Engineering
Biomedical Engineer, Medical Device Industry, Quality Engineering, Product Engineer
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 DescriptionVery 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 OpenPlanned Project
Top Must Have SkillsDOE/SPC process optimization & validation (IQ, OQ, PQ), FMEA.
Nice to have: packaging process experience
Day to Day ResponsibilitiesPosition 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.
- 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
- Quality System Regulation 21
- 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!!!
Not flexible for the working shift/hours required and limitation to travel. Approximately 1-2x per month
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