Process Engineer II

Marmon Holdings•Angola, IN

2d•Onsite

About The Position

Precision Edge Surgical Products Company LLC As a part of the global industrial organization Marmon Holdings—which is backed by Berkshire Hathaway— you’ll be doing things that matter, leading at every level, and winning a better way. We’re committed to making a positive impact on the world, providing you with diverse learning and working opportunities, and fostering a culture where everyone’s empowered to be their best. Welcome to Precision Edge Surgical Products! Precision Edge is a world-renowned contract manufacturer of fine surgical components, cutting tools and accessories. As a surgical cutting tool manufacturer, we pride ourselves in our technical versatility and ability to assist our customers. We understand the fundamental requirement of superior performance from a surgical instrument and our team takes extreme pride in building quality products which provide a competitive edge for our customers. We are currently hiring for a Process Engineer II in our Angola, Indiana location. If you meet the requirements below, we welcome you to apply.

Requirements

BS in Engineering required
2+ years engineering experience
Applied experience in AutoCAD, Solidworks or equivalent
Basic understanding of Geometric Dimensioning and Tolerancing (GD&T)
Ability to lift 50 pounds

Nice To Haves

Basic understanding of Validation, APQP or PPAP process desired
Understanding of statistical tools such as control charts, trending and capability analysis
Experience in Medical Device industry desired
Knowledge of Quality Management System standards (ISO, TS, FDA)
Understanding of Risk Management and the creation of tools such as FMEA

Responsibilities

Develop and implement production fixtures
Develop new Routers, Bill of Materials (BOM’s) and Inspection Instruction Sheets (IIS’)
Participate in the Material Review Board (MRB) with regards to internal NCR’s
Participate in corrective and preventive action activities on Customer Complaints
Utilize metrics to analyze repeated quality issues
Lead cell level process improvement initiatives and implement lean tools
Review product design for manufacturability for quoting
Manage all manufacturing details of New Products Release (NPRs)
Coordinate and conduct Pre-Production Reviews
Develop and execute Validation protocols and reports
Develop and implement inspection and gauging methods
Implement and improve upon existing manufacturing process
Communicate effectively with Cross Functional Team (CFT), customers and suppliers
Manage multiple tasks with limited supervision
Train employees as needed
Authorized to approve product realization (Engineering Activities) documentation in the absence of the Manufacturing and Quality Engineering Manager & Manufacturing Engineering Manager.