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Sr Design Quality Engineer at Strivector

Sr Design Quality Engineer

Strivector Naples, FL Full-Time
BE THE CHOICE, NOT THE OPTION
Strivector specializes in catering to your specific desired company culture and purpose-filled job needs.

We help our clients meet their fast-growing business, new and existing positions with talented individuals like you.

Strivector works alongside Fortune 500, mid-sized and Start-ups for full-time and contract positions; on our list of companies, we have Bank of America, Fannie Mae, Philips, Smith & Nephew, Arthrex.

THE EMPLOYER
Take your career up a few notches with a global medical device company and a leader in new product development and medical education in orthopaedics.

THE JOB
This is a Sr Design Quality Engineer position and requires someone who has Design Control/ Risk Management experience for this role . As a Sr Design Quality Engineer your roles and responsibilities will include:
  • Responsible for interfacing and driving Design Assurance principles within engineering teams for design, development transfer and post-market surveillance of FDA Class I and II, EU Class I, IIa, IIb and III medical devices in the achievement of company goals.
  • Lead design assurance efforts within product design and development for new product introduction projects with an emphasis in quality aspects of integrated software, electrical, and/or mechanical device characteristics, as appropriate for the specific area of position focus.
  • For electrical equipment / active device projects, lead compliance efforts for electrical safety, environmental, and emissions in accordance with national and international regulations.
  • Ensure appropriateness of documented design requirements and outputs while ensuring traceability throughout the product development lifecycle.
  • Provide active leadership in understanding and implementing regulations/standards, acting as a resource to other disciplines, within the product design process from idealization through product retirement.
  • Supervise, assign, and coordinate others / the work of others within the design assurance team to support the department and design projects and goals.
  • Provide input into and lead addressing of lessons learned to support development, modification, and improvement of design processes and quality management system.
  • Lead product risk assessment activities through application of a working knowledge of applicable standards (e.g., ISO14971, etc.) and tools such as (application, design, process) FMEAs, FTA, and Hazard Assessment.
  • Display working knowledge and provide guidance to design teams in the area of usability/human factors engineering principles including standards (IEC 62366) and FDA guidance for compliance.
  • Facilitate the planning, execution, and review of verification/validation (v&v) activities including assessment of adequate inputs to the v&v process.
  • Lead and coordinate the design assurance aspects of Design to Manufacture Transfer including generation of inspection methods, drawing reviews, determining key product indicators/essential requirements and, where appropriate, training of manufacturing personnel in appropriate test procedures, inspection methods, and interpretation of results.
  • Ensure required outputs of the design control process are met, including compliance of the design history file (DHF), and support transition of the design project into sustaining engineering.
  • Support design-related corrective and preventative activities for projects in the pre-sustaining phase.
Incidental Duties:
The above statements describe the general nature and level of work being performed in this job. They are not intended to be an exhaustive list of all duties, and indeed additional responsibilities may be assigned, as required, by management.

Education and Experience:
  • Bachelor s degree in Engineering required; Biomedical, Mechanical, or Electrical Engineering degree preferred.
  • 5 years design assurance / quality assurance experience in a medical device or other highly regulated industry required.
Knowledge and Skill Requirements/Specialized Courses and/or Training:
  • Working knowledge of ISO and FDA design and development quality requirements.
  • Technical knowledge in development methodologies, design quality analysis, and project implementation.
  • Proficiency in assessing manufacturing quality requirements of new product concepts.
  • Technical knowledge in development methodologies, design, and project implementation, including but not limited to, GD&T & DOE preferred.
Machine, Tools, and/or Equipment Skills:
Proficiency with PC operations, and the Microsoft Office suite, and CAD/CAM Software. Hands on experience with SAP and Agile preferred.

We understand that even if you are a seasoned Sr Design Quality Engineer you may not have all the skills listed here. If you are a good at what you do and have a willingness to learn, lets talk.


ADDITIONAL INFORMATION
Compensation: Based on Experience. One of the best in the industry
Minimum Education: Engineering Degree
Minimum Experience: 5 years of Design quality experience
Type of position: Full time Permanent Position with benefits
Telecommute: Yes
Location: Naples, FL
Relocation accepted: Yes

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