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Sr Design Assurance Quality Engineer - Hardware

Medtronic
Northridge, CA 91325
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Sr Design Assurance Quality Engineer - Hardware

Location:

Northridge, California, United States

Requisition #:

19000FCE

Post Date:

Dec 03, 2019


**Careers That Change Lives**


In this exciting role as a Senior Design AssuranceQuality Engineer - Hardware, you will serve as a subject matter expert by providing technical design quality support for the new product development and sustaining projects. The individual will act as a subject matter expert and provide guidance to the business in interpreting and executing against Medtronic quality system elements including hardware/system related work products to ensure compliance. This individual will ensure that all system-level project / program work products (e.g., plans, requirements, specifications, tests, test results, traceability, risk management documents, reports) meet Medtronics quality, reliability, and compliance requirements. This individual will ensure Design Quality Assurance-driven initiatives meet objectives in delivering highest quality products, with supporting tools and processes.


**DIABETES**


Transforming diabetes care together, for greater freedom and better health.


Our strategy is to become a holistic diabetes management company focused on making a real difference in outcomes and cost. We want to transform healthcare toward value-based models by driving both product and business model innovation with the goal of elevating patient experience, improving clinical outcomes and lowering the total cost of care for our customers.


We value what makes you unique. Be a part of a company that thinks differently to solve problems, make progress, and deliver meaningful innovations.


Visit www.medtronicdiabetes.com at http://www.medtronicdiabetes.com/ to see an overview of the products in our Diabetes product portfolio.


**A Day in the Life**


+ Leading large and complex medical device product development per the FDA design controls starting from design planning through design transfer.


+ Play a hands-on role in design transfer planning and ensure design transfer to manufacturing by supporting manufacturing process development qualification for transitioning development projects to manufacturing across multiple Medtronic sites and quality systems.

+ Generating master validation plans/reports and design transfer activities, including transitioning development projects to manufacturing.

+ Use of statistical techniques or data analysis and conclusions for deliverables like design verification reports/ process validation activities.

+ Generating and driving risk management deliverables like DFMEA/PFMEA and Hazard Analysis and preferably experienced in facilitation / execution of the process or design FMEAs.

+ Collaborating with the various product development teams like RD, Ops, Design / Supplier quality, risk management etc. to ensure work products comply with Medtronic procedures, acceptable qualitative and quantitative criteria, and global standards and regulations.

+ Assisting Supplier Quality Assurance with supplier audits; interfaces with Purchasing and Supplier Quality Assurance with supplier issues.

+ Leading and driving Design transfer activities and transitioning development projects to manufacturing smoothly.

+ Chair cross-functional change control boards.

+ Training and coaching cross-functional peers on maintaining compliance to internal and external Quality requirements and regulations in support of the deployment of the different BU strategies and products.

+ Driving clarity and consistency in documentation.

+ Leading CAPA projects and assisting post market analysis.

+ Participating in support of external regulatory audits and inspections.

+ Driving Process improvement activities.

+ Work under consultative direction toward predetermined long-range goals and objectives. Assignments are often self-initiated. Determine and pursue courses of action necessary to obtain desired results through consultation and agreement with others rather than by formal review of superior.

+ Performs other related duties as assigned.

+ Develops, modifies, applies and maintains quality standards and protocol for processing materials into partially finished or finished materials product.

+ Collaborates with engineering and manufacturing functions to ensure quality standards are in place.

+ Devises and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment.

+ Designs or specifies inspection and testing mechanisms and equipment; conducts quality assurance tests; and performs statistical analysis to assess the cost of and determine the responsibility for products or materials that do not meet required standards and specifications.

+ Ensures that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements.

+ May specialize in the areas of design, incoming material, production control, product evaluation and reliability, inventory control and/or research and development as they apply to product or process quality.


**Must Have: Minimum Requirements**


+ Bachelors Degree in Engineering, Science or technical field with 4+ years of work experience in Engineering and/or Quality OR Advanced Degree Engineering, Science or technical field with 2+ years of work experience in Engineering and/or Quality.


+ Experience working in a regulated industry (e.g., FDA-regulated).


**Nice to Have (Preferred Qualifications)**


+ Bachelors Degree in Biomedical or Electrical preferred.

+ Masters Degree in Engineering, Quality, Regulatory, or related.

+ ASQ Certification in Quality or Reliability.

+ Strong understanding and hands on experience with the FDA production and process controls (PPC), experience in planning of process validation / test method validation activities.

+ Working knowledge of ISO 13485, ISO 14971, 21 CFR 820, IEC 62304, IEC 60601-1 and MDD.

+ Understanding of the interdependencies of program work products and guide the teams in execution strategy and reviewing the program work products (e.g. plans, requirements, specifications, tests, test results, traceability, risk management documents, reports).

+ Experience with planning and executing design verification testing, test method development and test method validation (hands on execution experience preferred).

+ Working knowledge of hardware development for medical devices.

+ Ability to author technical reports, business correspondence and standard operating procedures.

+ Ability to apply knowledge and work with development and supply vendors to ensure compliance to Medtronic requirements.

+ Strong verbal and written English communication skills with an ability to effectively communicate at multiple hierarchal levels in the organization.

+ Ability to multi-tasks, prioritize, meets/exceed deadlines and hold themselves, and others accountable.

+ Self-Starter with a sharp focus on quality and customer experience.


**About Medtronic**


Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be.


We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Lets work together to address universal healthcare needs and improve patients lives. Help us shape the future.


Physical Job Requirements


The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role. (ADA-United States of America)
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.

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Posted: 2019-08-27 Expires: 2020-02-10
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Sr Design Assurance Quality Engineer - Hardware

Medtronic
Northridge, CA 91325

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