Entry-Level Medical Device R&D Engineer

MillenniumSoft Inc; Tempe (AZ); On-site; USD 28,000 - 41,000; Full time

Job summary

Medical Device Company in Tempe, AZ is seeking an Entry Level R&D Engineer on a 12-month contract (W2). The role supports R&D process development, testing, and data-driven improvements for medical device projects.

Responsibilities include coordinating prototype builds, setting up manufacturing equipment, developing processes, documenting SOPs and technical reports to GMP standards, performing test method development, and training manufacturing and QA personnel.

Qualifications

• Proficiency in MS Windows, Outlook, Word, Excel, and PowerPoint; data entry in MS Project and Minitab.
• Ability to analyze data and perform root-cause and statistical analysis.
• Ability to manage priorities with minimal supervision.
• Strong written and verbal communication; clearly convey status.

Responsibilities

• Assist in building product parts and prototypes for engineering evaluation and studies.
• Set up and operate manufacturing equipment.
• Develop new processes for medical devices and tooling.
• Support fixture, tooling, and equipment design and procurement.
• Prepare documents including work instructions, SOPs, reports that meet GMP/Quality requirements.
• Assist in test method development and validations.
• Perform tests, collect data, and present results as required.
• Provide training on processes and methods to manufacturing and QA.

Skills

Written communication

Verbal communication

Data analysis

Prioritization

Education

Associates degree in science/engineering

High school diploma

Tools

MS Project

Minitab

Solidworks

Job description

Medical Device Company in Tempe, AZ is seeking an Entry Level R&D Engineer on a 12-month contract (W2). The role supports R&D process development, testing, and data-driven improvements for medical device projects.

Responsibilities include coordinating prototype builds, setting up manufacturing equipment, developing processes, documenting SOPs and technical reports to GMP standards, performing test method development, and training manufacturing and QA personnel.