Associate Process Engineer

AtriCure • Mason, OH

18h

About The Position

The Associate Process Engineer is responsible for on-going production, validations, and continuous improvement of new and existing manufacturing processes. He/she contributes in a creative and collaborative ways to achieve the company’s goals of producing market leading products through positive patient outcomes.

Requirements

• Bachelor’s degree in Engineering or related field required
• 0-7 years of relevant experience.
• Able to assist the lead engineer for process improvement projects with minimal guidance
• Demonstrated Mechanical and/or Process Engineering ability.
• Understanding of external standards, design controls, quality controls, manufacturing methods.
• Demonstrates the ability to plan and track tasks to align with project plan and team objectives.
• Demonstrates excellent written and oral communication skills.
• Demonstrates excellent ability to work on and influence cross functional teams.
• Demonstrated ability with data analysis, problem-solving, and troubleshooting.
• Capable of prioritizing tasks and provide a timely schedule of completion.
• Ability to regularly walk, sit, or stand as needed
• Ability to occasionally bend and push/pull as needed
• Ability to regularly lift up to 10 pounds, occasionally lift up to 50 pounds
• Ability to pass pre-employment drug screen and background check

Nice To Haves

• Medical device industry experience
• Validation experience
• Understanding of Industry regulations as it pertains to medical devices
• Graduate degree
• Assembly and machining experience
• Regulatory experience
• Statistical use experience
• Engineering/design background
• Financial analysis experience

Responsibilities

• Team member of projects involving design, manufacturing, and quality resources, both internal and external.
• Support of product assembly line technical performance. Support production with troubleshooting assembly line issues, resolution of non-conformances, completion of root cause investigations, and CAPA’s.
• Collaborate with cross-functional engineering team (quality, product development, regulatory) to address product line issues.
• Responsible for communication of manufacturing and process issues to cross functional engineering team and suppliers, both verbally and in written documentation.
• Review of proposed component tolerances and input to manufacturing capability. Has knowledge of tolerance capabilities of machining, molding, casting, stamping, forming, grinding, etc. Understands GD&T and how to properly apply it to yield the desired fits between joining parts.
• Review of proposed device assembly requirements and identification of Design for Assembly opportunities. Understanding of assembly and joining techniques including laser welding, ultrasonic welding, adhesive bonding, over-molding, soldering etc. Understand of error proofing, poke-yoke.
• Knowledge of Manual and Automated Assembly Systems and Technologies.
• Knowledge of general manufacturing technologies (plastic injection molding, stamping, milling, turning, assembly methods, various fastening techniques) including low to medium volume manufacturing processes.
• Work with outside suppliers to define, document, analyze and qualify their manufacturing processes
• Identify new vendors, processes, materials, and technologies that can be used to improve product quality and reduce product cost
• Identify and implement manufacturing and product-related cost reduction opportunities. Understand life cycle costs and cost benefit analysis. Apply continuous improvement methods to enhance yield, consistency, performance, capacity, etc. of equipment and processes.
• Familiar with manufacturing efficiency strategies such as Lean, Six Sigma, 5S, Value Stream mapping, using SPC in resolving/improving productivity and efficiencies etc.
• Perform process capability assessments and establish methods to control process output.
• Working understanding of quality statistical models and metrics (confidence/reliability intervals, DOE, regression/trending, SPC, t-Tests, acceptance plans).
• Able to work in a controlled environment where gowning and strict adherence to clean room procedures are required.
• Able to define, communicate, and develop fixture concepts using internal and external resources. Able to incorporate the capabilities of typical production association into these concepts
• Work with designers and engineers in the design and development of manufacturing-related equipment and fixtures.
• Define and track project tooling and equipment schedule and cost
• Responsible for proper installation of new equipment and setting up proper preventive maintenance and calibration plans.
• Working knowledge of Manual and Automated Assembly Systems and Technologies, including both mechanical and control systems
• Experienced with mechanical equipment and gauges such as microscopes, soldering stations, ovens/furnaces, UV curing stations, Instron, calipers and other measurement gauges.
• Supporting process qualification strategies. Able to define statistical sample sizes as related to variable and attribute data based on established company and industry standards.
• Responsible for maintaining and updating Process maps and FMEAs.
• Responsible for writing and executing process qualification protocols and reports. Understanding of Test Method Validation, IQ, OQ, PQ approach as defined by AtriCure Quality System.
• Understand supply chains, lead times, and raw material availability
• Able to construct Bills of Material, with proper unit of measure and inventory points
• Knowledge of MRP and other requirement planning systems
• Able to conduct time studies and analyze cost variances
• Responsible for evaluating components for conformance to design intent via inspection and functional evaluation
• Responsible for trending scrap and failure rates, analyzing failure modes, and developing plans to address root cause issues
• Responsible for supporting ongoing manufacturing on a daily basis to allow them to meet required production goals
• Responsible for disposition of non-conforming material
• Properly document all work in compliance with AtriCure Quality System requirements
• Responsible for process documentation release using tools such as Visio, Excel, Word, Procal and Master Control documentation release systems
• Write detailed, easy to understand process instructions
• Write detailed test protocols and reports to document qualification activities
• Regular and predictable work performance
• Ability to work under fast-paced conditions
• Ability to make decisions and use good judgment
• Ability to prioritize various duties and multitask as required
• Ability to successfully work with others
• Additional duties as assigned

Benefits

• Medical & Dental beginning day 1 of employment
• 401K plus match
• 20 days of paid Parental Leave, in addition to maternity leave, for new moms and dads
• Volunteer Time off
• Pet Insurance
• full access to our on-site fitness center and cafeteria

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level