ZipRecruiter

Log In

3 Key Consulting
3 Key Consulting

62 3 Key Consulting Engineer 1 Jobs Hiring Near You

BayOne

Consulting Engineer 1

San Jose, CA · On-site

Minimum Requirements: ("Must have" Qualifications) 1. B.S. in Mechanical Engineering with 2+ years ... and data collection. 3. Hands-on laboratory experience in system assembly, setup, and ...

Neo4j

Consulting Engineer

San Mateo, CA · On-site +1

Key Responsibilities: * Work closely with customer engineering teams to lead and contribute to ... Competence and hands-on experience in at least one of the following languages: Java, JavaScript ...

BayOne

Consulting Engineer 3

Allentown, PA · On-site

$125K/yr

Description: Request #: 192664-1 Job Title: ASIC Verification Engineer Looking for how many ... Key Job Responsibilities Develop and implement Universal Verification Methodology (UVM) based ...

4P Consulting Inc.

ENGINEER 1

Atlanta, GA

HI, Hope you're doing well This is Pankaj from 4P Consulting I got your resume from career builder Please see below Job Title :: ENG1 Engineer 1 Location :: Atlanta, GA 30309 (ONSITE) Contract :: 24 ...

NxT Level

Structural Project Engineer

Raleigh, NC · Hybrid

$77K - $104K/yr

... be the key consulting engineer for residential and commercial construction clients. You will ... Minimum of 1 year of related experience. * North Carolina Engineering Intern (EI) Certification.

AMS Ameren Services

Consulting Engineer

Saint Louis, MO · On-site

$111K - $172K/yr

Key responsibilities include: * Develop engineering solutions, cost estimates, schedules and ... E.) License or commitment to actively pursue one in Illinois and/or Missouri required. Two or more ...

New

next page

Showing results 1-20

All Jobs3 Key Consulting Jobs3 Key Consulting Engineer 1 Jobs

3 Key Consulting Jobs Information

What other companies are hiring for Engineer 1 jobs?

What are the most popular jobs at 3 Key Consulting?

What are the most popular categories at 3 Key Consulting?

Infographic showing various Engineer 1 job openings at 3 Key Consulting in the United States as of August 2026, with employment types broken down into 96% Full Time, 2% Contract, and 2% Nights. Highlights an 78% Physical, 19% Hybrid, and 3% Remote job distribution.

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

3 Key Consulting

New Albany, OH

$52 - $57/hr

Full-time

Re-posted 12 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.