Sr. R&D Engineer

Gentuity

Sudbury, MA, United States2w ago

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Key details

Location
Sudbury, MA, United States
Work style
Onsite
Level
Senior
Experience
8–11 yrs
Function
Software engineering
Focus area
other
Posted
2w ago

Skills

design controlsdesign verificationengineering drawingsinjection moldingmanufacturing processespfmeastatistical modelingwelding

About the role

Description

The primary objective of this role is to advance HF-OCT catheter products through the product development lifecycle, from concept and design through verification, design transfer, and commercialization, resulting in best-in-class clinical and technical performance.


SUMMARY OF PRIMARY DUTIES AND RESPONSIBILITIES:

• Makes significant contributions to the product development of single-use intravascular devices, components, and related manufacturing methods with internal and external partners.

• Lead and/or support activities such as, design optimization, verification and validation testing, and design transfer.

• Drive technical decision making with internal and external teams, resolving design, manufacturing, supplier, and testing challenges as they arise, to ensure successful product development and company objectives are met.

• Support the creation and review of design verification test protocols and reports, design of experiments, and risk management file deliverables such as hazard analyses, FMEAs, etc.

• Ensure adherence to established design control processes, good engineering practices, and the company quality policy.

Other duties as assigned


Requirements

Minimum of 8+ years of technical design and medical product development experience with a four-year technical degree or 4-6 years with an advanced degree. A working knowledge in the following areas:


· Experience developing single use medical devices through design verification, validation, design transfer, and commercial release.

· Management of external partnerships for development and manufacturing

· Development of engineering drawings, specifications, tolerance analyses, and manufacturing documentation.

· Medical device design controls or equivalent via work in highly regulated industries

· Risk management processes including d/pFMEA, specification traceability, hazards analysis and statistical treatment of risks

· Development and execution of verifications strategies, test methods, protocols, statistical justifications, and technical reports.

· Application of statistical methods to verification planning, capability assessment, tolerance allocation, and design decision making.

· Catheter, balloon, and guidewire manufacturing processes including injection molding, extrusions, RF and ultrasonic welding, adhesives, laser processing, etc.

· Leadership/mentorship

· Analytic approach to design development including first principles analyses, finite element simulations, statistical modeling, etc.


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