Engineer Principal, Medical Device Development & Packaging C&Q - (JP14217) at 3 Key Consulting [...]

Engineer Principal, Medical Device Development & Packaging C&Q - (JP14217) job at 3 Key Consulting. New Albany, OH.

Job Title: Engineer Principal, Medical Device Development & Packaging C&Q - (JP14217)

Location: New Albany, OH. 43054

Employment Type: Contract

Business Unit: Site Process development

Duration: 1+ years (with possible extension)

Posting Date: 07/07/25

Pay Rate: $51 - $56/hour W2

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.

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 candidate 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. Responsibilities include:

• 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:

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