Quality Engineer 3

Job Description

Organization: Siemens Healthineers
Business Unit: Diagnostic Imaging
Requisition Number: 243736
Primary Location: United States-Illinois-Hoffman Estates
Assignment Category: Full-time regular
Experience Level: Mid level
Education Required Level: Bachelor's Degree
Travel Required: 5%

Division Description:

At Siemens Healthineers, we are passionate about enabling healthcare professionals to deliver high quality patient care, and to do so affordably.  A leading global healthcare company, Siemens Healthineers continues to strengthen our portfolio of medical imaging and laboratory diagnostics, while adding new offerings such as managed services, consulting, and healthcare IT services – as well as further technologies in the growing market for therapeutic and molecular diagnostics.


Siemens Healthineers develops innovations that support better patient outcomes with greater efficiencies, giving providers the confidence they need to meet the clinical, operational and financial challenges of a changing healthcare landscape.


Job Description:

Position Overview


Participates in formulating quality programs, plans, procedures and practices. Performs semi-complex statistical analysis as related to product and material quality. Supports in the analysis of defective material and leads in the final disposition of defective material through the material review board process. Analyze production and material review board data to determine trends to initiate corrective action and identify continuous improvement opportunities. Conducts semi-complex audits of supplier quality system or manufacturing processes to determine compliance with our quality requirements. Provides monthly performance input to the supplier rating system. Provides input during new supplier evaluation to determine suitability for inclusion to the Approved Supplier List ( ASL). Maintains the required views in the SAP ERP system including inspection planning. Provides technical in-put, training and guidance to inspectors.



Primary responsibilities include the approval, development and management of all direct and indirect quality relevant material suppliers, and to ensure the material received from them is conforming.


Work cross-functionally in support of product development to ensure that that the supply chain is fully qualified before product release.


Review design specifications and develop material inspection plans within the SAP ERP system to be used incoming inspection personnel to assess the conformance of received material.  Provide assistance and guidance to inspection personnel as needed. 


Develop and maintain supplier performance KPI’s and utilize them assess quality trends, performance target setting and verify effectiveness of implemented corrective action plans.


Analyze the complexities and interrelationships of non-conforming material situations and determine the root cause as well what an effective corrective action plan would entail. Evaluate 8D responses from suppliers to formal corrective action requests (SCARs) for thoroughness and effectiveness.


Proficiently use of basic statistical analysis methods and practices to analyze processes and corrective action plans to determine the state of control or effectiveness.


Conduct on site supplier QMS and or process audits and drive corrective action plans


Excellent decision making abilities showing awareness of risk and regulatory requirements. Able to evaluate options and solutions while using good judgment.


Required Knowledge/Skills, Education, and Experience


Must have an accumulated 5 to 10 years of successful experience in quality disciplines or related field, and successful demonstration of key responsibilities and job knowledge.  Must have a BS degree in a technical field, ME, EE, or IE preferred.

Preferred Knowledge/Skills, Education, and Experience


Experienced in performing both quality system and product audits performed at a supplier or subcontractor facility both domestic and internationally.   Have obtained sufficient audit training from an accredited source (ASQ or ANSI-RAB NAP) resulting in an ASQ-CQA or RAB certification.


Achieved and maintained ASQ-CQE certification


Knowledge / training of ISO 13485 and ISO 9000


Received training and successfully implemented quality assurance methodology to analyze and control key process parameters (Six Sigma, SPC, gage R&R, FMEA, and Poke –Yoke, etc.)


Proficient with Microsoft Office with emphasis on EXCEL.  Minitab experience would be a plus.


Equal Employment Opportunity Statement
Siemens is an Equal Opportunity and Affirmative Action Employer encouraging diversity in the workplace. All qualified applicants will receive consideration for employment without regard to their race, color, creed, religion, national origin, citizenship status, ancestry, sex, age, physical or mental disability, marital status, family responsibilities, pregnancy, genetic information, sexual orientation, gender expression, gender identity, transgender, sex stereotyping, protected veteran or military status, and other categories protected by federal, state or local law.

EEO is the Law
Applicants and employees are protected under Federal law from discrimination. To learn more, Click here.

Pay Transparency Non-Discrimination Provision
Siemens follows Executive Order 11246, including the Pay Transparency Nondiscrimination Provision. To learn more, Click here.

Can't find what you are looking for?

Let's stay connected

Can't find what you are looking for?