We are a contract manufacturer that improves patient's lives by partnering with leading orthopedic companies to develop and manufacture complex surgical cutting tools and instruments. Our partners confidently rely on our industry leading technical services to add value to their original designs and improve surgical outcomes and manufacturability.
Our Vision:
To be the trusted technical leader and first-choice strategic outsourcing partner in the development and manufacturing of complex surgical products for the leading orthopedic companies
The Role: Process Engineer II
Precision Edge Surgical Products LLC of Angola, Indiana is looking to hire a full-time Process Engineer II. Are you looking for a long-term career with a stable manufacturing company that will value you? If so, please read on!
This engineering position earns competitive pay. We also provide great benefits and perks starting on day one of employment, including health, dental, vision, company-paid short- and long-term disability, company-paid life, company-paid accidental death and dismemberment (AD&D), voluntary life, paid vacations, and paid holidays. Additionally, we offer a 401(k) plan with a 50% company match up to 3%, starting on the first of the month following 30 days of employment. If this sounds like the right opportunity in the medical device industry for you, apply today!
A DAY IN THE LIFE OF A PROCESS ENGINEER II
As a Process Engineer II, you ensure that our manufacturing facilities run smoothly every day while proactively planning for future needs and growth. You develop new routers, bills of materials, and inspection instruction sheets as well as participate as a member of the material review board. Using statistical process control (SPC) methods, you lead and implement process improvement initiatives for our manufacturing operations. You also evaluate the frequency of inspections as well as develop inspection and gauging methods.
Additionally, you are involved in the development of our medical devices by reviewing product designs, coordinating and conducting pre-production reviews, and managing the manufacturing details of new product releases (NPRs). You also assist in our efforts to correct and prevent customer complaints as well as execute validation protocols. You feel great about increasing value in our manufacturing facilities by bringing solutions to complex problems and finding ways to improve our processes and medical device products!
QUALIFICATIONS
Bachelor of Science degree in engineering
Experience using AutoCAD, SolidWorks, or related software
Basic understanding of geometric dimensioning and tolerancing (GD&T)
Understanding of statistical tools such as control charts and capability analysis systems
Knowledge about quality management system standards
Understanding of risk management and the creation of tools such as failure mode & effects analysis (FMEA)
3+ years of engineering experience, as well as experience with CNC machining processes or in the medical device industry, is preferred but not required. A basic understanding of validation, production part approval process (PPAP), or advanced product quality planning (APQP) would be a plus.
Do you take pride in your work? Are you analytical and detail-oriented? Do you have excellent communication skills, both written and verbal? If so, you might just be perfect for this position.
In addition to a competitive salary, our total rewards package includes:
Market competitive medical, vision and dental benefits beginning on day one.
Life and disability insurance (short and long term).
A competitive 401k plan that has both matching and non-matching company contributions.
Paid time off to include annual PTO as well as company paid holidays.