Co-Op, Production Engineering

Getinge•Wayne, NJ

1d•Hybrid

About The Position

This is a co-op position where the individual will be supervised and trained by Reporting Supervisor and Engineering personnel. Projects will start with close supervision and small scope, gradually progressing to larger and more complex tasks. Responsibilities will increase based on the individual's experience and willingness to learn new aspects of manufacturing engineering. The position is expected to last for approximately one year, starting in spring 2026 and concluding in spring 2027. The role involves a hybrid work schedule, requiring 3-4 days per week in the office in Wayne, NJ, with a total of 35-40 hours per week.

Requirements

2+ academic years of education in an engineering curriculum; Mechanical, Biomedical, Electrical Engineering, or similar.
Proficiency with CAD tools like SolidWorks, AutoCAD, Fusion 360, etc.
Ability to work 35 - 40 hour per week
Knowledge of using various measurement devices such as micrometers, calipers, and thickness gages, optical measuring systems, Instron testers.
Ability to read and interpret Engineering drawings.
Good communication skills, both written and verbal.
Must have good manual dexterity to work with small parts.
Detail oriented with good mechanical aptitude and good technical writing skills.
Work in a lab environment where extensive time sitting may be required.
Knowledge of Statistical analysis.
Work under the supervision of Production Engineering Supervisor or Production Engineers.
Computer skills including, but not limited to: Microsoft Windows, Word, Excel

Responsibilities

Provide technical support to the Production Engineering staff for development of new processes and products.
Complete routine assignments where some judgment is required for a successful outcome.
Complete documentation updates in Document Management System (engineering specifications, change notices, manufacturing standard operating procedures, tooling/fixture drawings, equipment maintenance specifications and registrations and other documentation).
Run standard and newly developed test protocols, compile and complete analysis of test data and materials testing.
Assist in performing/executing various protocols for process validations including but not limited to pull testing, measuring and use of gages, visual evaluations.
Assist in performing packaging material artwork verification (Instruction for Use, Labels, Pouches, Carton tops and bottoms).
Write test procedures and validations protocols.
Use of Statistical Analysis (Minitab software) in summarizing validation protocols.
Document experimental records in lab notebook.
Comply with Quality System Procedures, Good Lab Practices, and Exposure Control Plan.
Troubleshoot fixtures and electronic equipment.