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NPI Process Development Engineer

Tegra Medical Holdings LLC
Posted 19 hours ago, valid for 9 days
Location

Franklin, MA 02038, US

Salary

$85,000 - $100,000 per year

Contract type

Full Time

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Sonic Summary

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  • The position of Product Development Engineer (PDE) focuses on transforming designs into high-quality medical products while reducing manufacturing costs.
  • Candidates should have at least four years of engineering experience and a bachelor's degree in mechanical or industrial engineering, or equivalent experience.
  • The role involves collaboration with various teams and customers, defining project scopes, and supporting project schedules to meet milestones.
  • PDEs are required to have strong interpersonal skills and experience with medical devices, including knowledge of ISO 13485 quality standards.
  • The position offers a competitive salary, which is not specified in the summary, and requires hands-on development activities in a dynamic work environment.

Job Summary

PDEs turn great designs into great products. Customers love our PDEs because they find ways to lower their manufacturing costs and make better quality products. They are experts in the science of efficient manufacturing and the art of using their “soft skills” – working closely with customers to negotiate and refine the tiniest details. In short, they know how to figure out the smartest way to manufacture a medical device and how to influence and guide colleagues, management, and customers.

As a PDE you might find yourself working on ground-breaking devices from head to toe including those for cardiac surgery, neuro implants, and sports medicine.

 

Role and Responsibilities

  • Work in a high visibility job in a global company, collaborating with people at all levels and functions within Tegra Medical and with our customers.
  • Help define the project scope and support project quoting, including process, material, and NRE estimation.
  • Develop, drive, and support the project schedule to maintain adherence to objectives and commitments.
  • Work collaboratively with Quality and Operations to develop, gain support, and meet project milestones.
  • Support hands-on development activities related to fabrication and assembly of customer products. This includes the creation of work Instructions, training requirements, and inspection methods.
  • Assist in the development and completion of required validation protocols, reports, and other quality activities and documentation.
  • Work through Tegra Medical’s program management system and drive projects to scaled production volumes.
  • Become a trusted member of the development team, working closely with the customer engineering team as you collaborate on refining their design for manufacturing.
  • Roll up your sleeves and put on your safety glasses as you put your ideas into action on the production floor.
  • There may be additional duties and responsibilities in this dynamic environment.


Level of Skill, Education and Experience

  • Four or more years of engineering experience
  • Bachelor’s degree in mechanical or industrial engineering, or equivalent experience
  • Great interpersonal and negotiation skills, particularly when working with customers
  • The ability to be relied on as a key team member
  • An eye for details and a passion for perfection Experience with medical devices and/or ISO 13485 quality standards
  • Process validations (IQ/OQ/PQ requirements)
  • Microsoft Project (Gantt charts)
  • SolidWorks training


Physical Requirements:

  • Frequent performing repetitive work
  • Frequent safety clothing required (safety glasses)
  • Constant PPE gowning 
  • Occasional lifting (max. 40 lbs.)
  • Occasional carrying (max. 40 lbs.)
  • Subject to physical hazards from moving equipment and machine parts
  • Frequent standing
  • Occasional sitting, walking, pushing, pulling, reaching

 


M-F Standard Office Hours



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