Staff Supplier Quality Engineer

We foster a culture of inclusion by embracing diverse experiences and individuals where everyone’s authentic self is welcome. We offer supporting programs and resources that provide enriching and equitable opportunities for each person to contribute professionally and personally. This Position is located in Mason/Cincinnati, OH and will be onsite. Must be able to commute daily or relocate to Cincinnati, OH to be considered. Relocation assistance is available.

POSITION SUMMARY

This position will be responsible for the development and implementation of supplier-related quality system requirements including compliance with international and domestic regulations in support of new product development, manufacturing, and quality management system activities with a focus on continuous improvement.

ESSENTIAL FUNCTIONS OF THE POSITION

Develop and maintain supplier-related procedures and requirements in compliance to FDA regulations, MDD, CMDR, and ISO requirements including evaluations, audits, and metrics Direct and support supplier-related activities, including: QMS qualification and monitoring leading supplier audits/assessments while training other auditors. Composes and drives timely completion of component (and sub-assembly) qualification elements such as defining requirements and assessing First Articles, Measurement Systems, equipment and process qualifications, Control Plans, etc. Correction activities including managing NCRs and SCARs, possibly including supplier education in these activities Manage and lead Supplier change requests and improvement Work closely with Quality Management and other departments in developing and executing company strategies – including possible leading of small group efforts. Work cross-functionally, overcome technical and logistical challenges, and facilitate cooperation with suppliers to meet regulatory requirements. Assist with FDA and ISO audits. As necessary, perform internal and supplier audits as Audit Lead. Strong working knowledge of domestic and international standards and controls relevant to the duties and expectations of this position Operates with appreciable latitude for, and assumes ownership of, and driving completion of actions and/or decisions on day-to-day activities. Determines appropriate response to novel or controversial problems that may impact the business significantly and presents plans to resolve such problems. Uses knowledge of best practices, technical proficiency, and past experiences in supplier quality engineering to mentor junior SQE’s. Other duties as necessary and assigned

ADDITIONAL ESSENTIAL FUNCTIONS OF THE POSITION

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

BASIC QUALIFICATIONS

Bachelor’s degree with 6+ years of experience in Quality Engineering (at least 3 in Supplier Quality) FDA and ISO 13485 knowledge and multiple audit experiences Willingness to travel (~25%) Demonstrated experience with inspection/testing and data analysis Strong computer/data entry, report writing, and communication skills. Greater use of tools above MS Office (ie. Visio, Power BI, etc) for communication and analysis. Statistical use experience – Assessing capability, running hypothesis tests Details-oriented with demonstrated problem solving/trouble shooting experience of larger magnitude. Must be able to read technical specifications, blueprints, and drawings. Working knowledge of GD&T Engineering/Manufacturing background – preferably machining, molding, and finishing processes

PREFERRED QUALIFICATIONS

Advanced degree MDD, CMDR and JPAL knowledge ASQ Certified Quality Engineer ASQ Certified Quality Auditor

OTHER REQUIREMENTS

Ability to regularly walk, sit, or stand as needed Ability to occasionally bend and push/pull as needed Ability to regularly lift up to 25 pounds, occasionally lift over 25 pounds Ability to pass pre-employment drug screen and background check

BENEFITS

AtriCure has a variety of benefits available for US based employees and their families. Examples include Medical & Dental beginning day 1 of employment, 401K plus match, 30 days of paid Parental Leave, in addition to maternity leave, for new moms and dads, Volunteer Time off, Pet Insurance, and more. Corporate-based employees also have full access to our on-site fitness center and cafeteria. To see a complete list of our benefits, please visit our careers website:

LEGAL NOTICE

AtriCure participates in the federal E-Verify program to confirm the identity of and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here AtriCure is an Equal Employment Opportunity/Affirmative Action employer and provides Drug Free Workplaces. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national or ethnic origin, age, protected veteran status, status as an individual with disability, sexual orientation, gender identity or any other characteristic protected by federal, state, or local law(s). #J-18808-Ljbffr AtriCure