Senior QA Engineer

Innovation that sparks imagination. Continue on to your next challenge with us. 

Carestream is a worldwide provider of medical imaging systems and solutions; x-ray imaging systems for non-destructive testing; manufacturing of film and precision contract coating services for a wide range of industrial, medical, electronic and other applications—all backed by a global service and support network. Carestream's diagnostic imaging technology systems are at work in 90 percent of hospitals worldwide.  

At Carestream, we offer a global perspective and a world of opportunities for people who have the desire to make a positive impact. Join our global team of 3,000+ professionals

Compensation: $90,000 - $105,000

*This range reflects Carestream's good faith estimate to pay fairly as starting wage. Offers will be tailored within the range based on the selected candidate's experience, industry knowledge, technical and communication skills, and other factors that may prove relevant during the interview process, as well as geographic market differentials for the position.

Within the NDT Research and Development team, the Senior Quality Assurance Engineer is responsible for system test design, planning, and oversight of test execution on a variety of system products which are comprised of electronic and electro- mechanical components with embedded software control.  The systems typically leverage common components including host application software (running on a windows PC) that provides the primary user interface with high level system coordination.  The systems are sold to customers working in support of the Non-Destructive Testing industry.

•    Responsible for supporting design verification of new product design, development, and transfer of the resultant design to manufacturing along with process compliance to regulatory requirements. 

•    Contributes to new product development/manufacturing in areas of design verification & validation of product requirements, regulatory requirements, specification development, measurable outcomes, hazard and safety analyses and other quality activities necessary to meet project objectives in the hardware/software/manufacturing arenas.

•    Leads product design teams through system Failure Mode Effects Analysis (FMEA) activities

•    Creates and executes test plans 

•    Develops schedules/resource plans for the verification and validation portion of a product design project

•    Documents and delivers to the appropriate repository all test results, analysis, and test summary reports 

•    Represents customer perspective in project quality decisions.

•    Provides clear scope definition, implements new tools, drives change management, and defines metrics that define successful completion.

•    Supporting Regulatory agency audits and inspections.

•    Leads verification activities related to design change activities including testing assignments on updates to existing products.

•    Duties may include leading cross-functional corrective action team(s) or projects

•    Duties may include activities to support the customer complaint process

•    Duties may include supplier quality and audit activities.

•    Bachelor's degree in Engineering (electrical or mechanical) or any STEM program.

•    Min 5 years of demonstrated engineering skills

•    Ability to provide direction to and apply statistical tools

•    Demonstrated data-driven decision making

•    Ability to influence within peer group and higher management

•    Excellent attention to detail

•    Leadership skills

•    Strong analytical, decision-making and problem-solving skills.

•    Excellent written and verbal communication

•    Quality Engineering, manufacturing or service experience within an ISO and/or FDA regulated medical device industry.

•    Knowledge of industry standards such as AWS, ASME, API (510, 570, 1169)

•    Working knowledge of MIL specs and NDE methodologies

•    Competent in the use of statistical software (ex. Minitab, Reliasoft, etc)

•    ASQ Certification (CQE, CRE), Six Sigma Black Belt or Green Belt Certification

•    Competent in the use of quality tools (ex. Reliability, FMEA, fault tree analysis, root cause analysis, fishbone diagrams, DOE, ANOVA, Cpk, etc)

Traditional Office Environment:  This position is primarily an office setting with standard temperature and humidity controls, moderate to light noise, fluorescent lighting, primarily sitting with standing desks available, extensive computer and keyboard use, etc.   

Carestream is an Equal Opportunity Employer

Carestream is an equal opportunity organization. We recruit, employ, train, compensate, and promote without regard to race, religion, creed, color, national origin, age, gender, sexual orientation, gender identity, marital status, disability, veteran status, or any other basis protected by applicable federal, state or local law.

Applying for a job with Carestream

All applicants must complete the on-line application process. Carestream is committed to working with and providing reasonable accommodations to individuals with disabilities. If you require assistance or an accommodation because of a disability to participate in the application process, please click accommodations

Requisition ID: 4605