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Product Development Engineer III - Sandy

Spectrum Plastics Group
Sandy, UT Other
POSTED ON 1/1/2025
AVAILABLE BEFORE 2/28/2025

Job Details

Job Location:    Apollo - Sandy - Sandy, UT
Position Type:    Full Time
Education Level:    4 Year Degree
Salary Range:    Undisclosed
Job Category:    Engineering

Description

JOB PURPOSE:

To design new devices/components and make design changes or improvements to existing devices/components. Leads major programs to bring new designs or design changes through the applicable phases of the Product Development Process.

 

ESSENTIAL DUTIES:

  • Functions as leader for major programs involving all phases of product design and development, leading Core Team through the execution of project activities
  • Follows and improves the Product Development Process to ensure regulatory requirements are met and that the medical device meets the requirements for its intended use
  • Plans and 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
  • Guides the project team through use of design and technology to drive innovation and significantly improve patient outcome
  • Strives for improvement to ensure 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 creation of detailed 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
  • Able to navigate completely new medical devices through product requirements, design inputs, design outputs, and verification/validation in traceability matrix
  • Introduces design mitigations to significantly reduce the risk profile for the medical device 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 expansive product lines and corresponding manufacturing processes while meeting expectations for sustainable, efficient, repeatable, and reproducible manufacturing operations
  • Leads Core Team to ensure that project phases are completed in a timely manner
  • Defines activities for project execution to meet the requirements of the Product Development Process
  • Supports request for quotes, specifically complex devices that vary greatly from predicates
  • Upholds Spectrum Plastics Group vision and core values
  • Follows all safety guidelines and adheres to safety absolutes

Qualifications


QUALIFICATIONS (Education/Experience/Knowledge, Skills & Abilities)

Required:

  • Bachelor’s degree in engineering or equivalent experience in a related field.
  • 7 years industry experience
  • Proficient in commonly-used concepts, practices, and procedures within  medical device design and development
  • 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
  • Can handle financial responsibilities for major programs, such as budget accountability and revenue recognition
  • 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 apply knowledge to their job function using pre-established guidelines and instructions
  • 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

Preferred:

  • Master’s Degree in Engineering discipline
  • Proficiency in Microsoft Project
  • Demonstrated ability to complete product design transfers
  • Knowledge of applicable standards for EtO sterilization (e.g. ANSI/AAMI/ISO 11135-1, ANSI/AAMI/ISO 11135-2)

 

WORKING CONDITIONS:

Works with minimal supervision from manager.  Requires light physical activity performing non-strenuous daily activities

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