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Product Development Engineer

Spectrum Plastics Group
Posted 3 months ago, valid for a month
Location

Tucson, AZ 85705, US

Salary

Competitive

Contract type

Full Time

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Sonic Summary

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  • The job at Xeridiem in Tucson, AZ, involves designing new medical devices and improving existing components, requiring a Bachelor's degree in engineering and 3-7 years of industry experience.
  • Responsibilities include leading projects through the Product Development Process, applying risk management policies, and ensuring design for manufacturability and usability.
  • Candidates must have a strong understanding of ISO 13485 requirements and demonstrate problem-solving skills, accuracy, and attention to detail.
  • The position offers a full-time salary, although the specific salary range is not provided in the job description.
  • Preferred qualifications include a Master's degree in Engineering and experience in project management within medical device design and development.

Job DetailsJob Location: Xeridiem - Tucson - Tucson, AZ 85714Position Type: Full TimeJOB PURPOSE: To design new devices/components and make design changes or improvements to existing devices/components. Leads or is a team member on projects to bring new designs or design changes through the applicable phases of the Product Development Process. ESSENTIAL DUTIES: Functions as leader or team member for projects involving all phases of product design and development, leading Core Team through the execution of project activities Drives execution of project activities through the applicable project phases to the final phase of Commercial Release for ongoing production Applies the Risk Management Policy to the development process for identifying hazards, estimating and evaluating associated risks, controlling these risks and monitoring the effectiveness of risk controls Optimizes design and technology to drive innovation and significantly improve patient outcome Ensures all applicable aspects of product design including design for manufacturability, scalability, testing, variability, and usability Diligently develops product requirements and design inputs based on the applicable standards as well as other relevant sources, such as Post-Market Surveillance Oversees and participates in creation of sub-assembly and final assembly drawings to serve as design specifications for a medical device Develops verification and validation plans for the protocols, test methods, and reports for execution of design verification and validation testing Verifies connection between product requirements, design inputs, design outputs, and verification/validation is clear in traceability matrix Leads and ensures thoroughness of risk management activities as documented in Risk Management File, dFMEA, and pFMEA (design/process Failure Mode Effects Analysis) Evaluates and designs products, parts, or processes for cost efficiency to minimize the cost for patient care Coordinates project activities for Commercial Release of product and corresponding manufacturing processes while meeting expectations for sustainable, efficient, repeatable, and reproducible manufacturing operations Defines activities for project execution to meet the requirements of the Product Development Process Supports requests for quotes by outlining necessary project activities and timing for new product introduction Upholds SPG and Dupont vision and core values Performs all other duties as assigned   QualificationsQUALIFICATIONS (Education/Experience/Knowledge, Skills & Abilities) Required: Bachelor's degree in engineering or equivalent experience in a related field. 3-7 years industry experience Demonstrated history to problem solve, identify errors and deficiencies and perform research High degree of understanding of ISO 13485 requirements for Design Controls Ability to provide guidelines and instructions applicable to the job function Accuracy, attention to detail, and thoroughness Proficient computer skills Proficient communications skills Ability to comprehend and comply with company safety and quality standards Ability to provide oral and written instructions to others Responsible for understanding and complying with all SPG and DuPont safety policies and procedures Preferred: Master’s degree in Engineering discipline Experience as project manager on a project which involved all phases of product design and development, leading Core Team through the execution of project activities Knowledge on developing full-scale project plans Effectively communicated project expectations to team members and stakeholders in a timely and clear fashion Experience planning and driving execution of project activities through the applicable project phases to the final phase of Commercial Release for ongoing production Has knowledge of commonly used concepts, practices, and procedures within medical device design and development Can handle financial responsibilities for project such as budget accountability and revenue recognition Experience developing Gantt Charts in Microsoft Project Demonstrated ability to complete product design transfers WORKING CONDITIONS: Works with supervision from manager as necessary.  Requires light physical activity performing non-strenuous daily activities. 




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