Process Engineer II

Process Engineer II page is loaded## Process Engineer II locations:
Angola, INtime type:
Full time posted on:
Posted Todayjob requisition :
JR Precision Edge Surgical Products Company LLCAs 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.
** DEPARTMENT:
** Engineering
*
* JOB TITLE:

** Process Engineer II
** SHIFT:
** Days
* * Benefits
* ** Benefits starting on Day 1
* Competitive Pay
* Company paid Short- and Long-Term Disability
* Company paid Life and AD&D Insurance
* Paid Time Off and Company Paid Holidays
* 401K with Company Match
* Climate Controlled, Clean Work Environment
** Education/Experience
*** BS in Engineering required
* 2+ years engineering experience
* Applied experience in AutoCAD, Solidworks or equivalent
* Basic understanding of Geometric Dimensioning and Tolerancing (GD&T)
* 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
** Responsibility/Authority
*** Develop and implement production fixtures
* Ability to lift 50 pounds
* 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.

Following receipt of a conditional offer of employment, candidates will be required to complete additional job-related screening processes as permitted or required by applicable law.

We are an equal opportunity employer, and all applicants will be considered for employment without attention to their membership in any protected class. If you require any reasonable accommodation to complete your application or any part of the recruiting process, please email your request to , and please be sure to include the title and the location of the position for which you are applying.

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