Quality Engineer

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A career at Flex offers the opportunity to make a difference and invest in your growth in a respectful, inclusive, and collaborative environment. If you are excited about a role but don't meet every bullet point, we encourage you to apply and join us to create the extraordinary.## ##

Job Summary To support our extraordinary teams who build great products and contribute to our growth, we’re looking to add a
** Quality Engineer
** located in
** Austin, TX.
** Reporting to the
** Quality Manager,
** the
** Quality Engineer
** will be to maintaining quality engineering programs, standards and improvements within the organization.
** What a typical day looks like:
*** Develops and initiates standards and methods for inspection, testing and evaluation.
* Devises sampling procedures and designs and develops forms and instructions for recording, evaluating and reporting quality and reliability data.
* Develops and implements methods and procedures for disposition of discrepant material and devises methods to assess cost.
* Directs workers engaged in measuring and testing product and tabulating data concerning materials, product or process quality and reliability.
* Compiles and writes training material and conducts training sessions on quality control activities.
* · Holds up Product Engineers and Quality Program Managers with customer interfaces as necessary on quality related issues.
* Assures data availability and integrity for all quality related data. Consolidates and reports quality results.
* Initiates corrective action requests as needed and tracks to satisfactory completion.
* Assists with development and implementation of quality audits.
* In charge of developing, applying, revising and maintaining quality standards for processing materials into partially finished or finished products.
* Designs and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and/or production equipment.
* Explores reports and returned products and recommends corrective action.
* Establishes program to evaluate precision and accuracy of production equipment and testing, measurement and research of equipment and facilities.
* Approves product, process and equipment qualifications.
* Provides liaison to various regulatory bodies
* Facilitate and lead customer-focused meetings to address quality and performance concerns.
* Manage and resolve quality issues including nonconformances, CAPAs, and deviations.
* Provide technical support for validation activities and ensure compliance with regulatory standards.
* Lead discussions on Good Manufacturing Practices (GMP) and drive process improvement initiatives.
* Organize and lead meetings focused on yield enhancement and scrap reduction strategies.
* Support Device History Record (DHR) investigations and related documentation.
* Oversee and execute risk management activities to mitigate potential quality and compliance risks.
** The experience we’re looking to add to our team:
*** Bachelor’s degree in related field or equivalent experience.
* 3+ years of experience as a Quality Engineering in the medical devices industry.
* Experience working on CAPA´s & DHR
* Advanced skills in Microsoft Excel and PowerPoint…