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Body Design Engineer Jobs in Boston, MA (NOW HIRING)

Will mentor and coach early career engineers and lead continuous improvement of the Design Engineering Body of Knowledge (BOK). Requirements and Considerations * Bachelor's Degree in Mechanical ...

Senior Industrial Design, Lead

Boston, MA

$110K - $118K/yr

... body types, activities, environments, and use cases. * Partner closely with Mechanical Engineering, Electrical Engineering, Sensors, Apparel, Product, and Manufacturing to balance design intent ...

Senior Industrial Design, Lead

Boston, MA · On-site

$110K - $118K/yr

... body types, activities, environments, and use cases. * Partner closely with Mechanical Engineering, Electrical Engineering, Sensors, Apparel, Product, and Manufacturing to balance design intent ...

Senior Industrial Design, Lead

Boston, MA · On-site

$110K - $118K/yr

... body types, activities, environments, and use cases. * Partner closely with Mechanical Engineering, Electrical Engineering, Sensors, Apparel, Product, and Manufacturing to balance design intent ...

Senior Industrial Design, Lead

Boston, MA · On-site

$110K - $118K/yr

... body types, activities, environments, and use cases. * Partner closely with Mechanical Engineering, Electrical Engineering, Sensors, Apparel, Product, and Manufacturing to balance design intent ...

Senior Staff Mechanical Engineer

Wilmington, MA · On-site

$114K - $150K/yr

Will mentor and coach early career engineers and lead continuous improvement of the Design Engineering Body of Knowledge (BOK). Requirements and Considerations * Bachelor's Degree in Mechanical ...

... and Notified Body or FDA feedback cycles. Assure that all activities related to product ... Systems Engineering to ISO 14971 risk management and design controls; Chemical/Materials ...

About Us SharkNinja is a global product design and technology company, with a diversified portfolio ... Notified Body or FDA feedback cycles. • Assure that all activities related to product ...

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Showing results 1-20

Body Design Engineer information

What is the difference between Body Design Engineer vs Structural Engineer?

AspectBody Design EngineerStructural Engineer
CredentialsBachelor's in Mechanical, Automotive, or Aerospace EngineeringBachelor's in Civil, Mechanical, or Structural Engineering
Work EnvironmentAutomotive, aerospace, or manufacturing industriesConstruction, infrastructure, or building projects
Industry UsageDesigning vehicle bodies, aircraft fuselages, or product shellsDesigning load-bearing structures for buildings and bridges

While both roles involve engineering design, a Body Design Engineer focuses on creating vehicle or product shells, emphasizing aerodynamics and aesthetics, whereas a Structural Engineer specializes in ensuring the safety and stability of buildings and infrastructure. Both roles require similar educational backgrounds and work in related industries, but their specific applications and design focus differ significantly.

What is a Body Design Engineer?

A Body Design Engineer is a professional who designs and develops the structural and exterior components of vehicles, such as doors, hoods, fenders, roofs, and frames. They focus on ensuring that these parts meet safety, durability, and aesthetic requirements while collaborating with other engineering teams. Body Design Engineers use computer-aided design (CAD) software and work closely with manufacturing to ensure that designs can be efficiently produced. Their role is essential in creating vehicles that are safe, functional, and visually appealing.

What are some common challenges faced by Body Design Engineers in automotive projects?

Body Design Engineers often encounter challenges such as balancing aesthetic requirements with structural integrity, meeting safety regulations, and integrating new materials or technologies. They must coordinate closely with cross-functional teams, including manufacturing, electrical, and safety engineers, to ensure that all design aspects are feasible for mass production and meet quality standards. Additionally, tight project timelines and evolving customer expectations can add complexity to the role, requiring strong problem-solving skills and adaptability.

What are the key skills and qualifications needed to thrive as a Body Design Engineer, and why are they important?

To thrive as a Body Design Engineer, you need a solid background in mechanical engineering, knowledge of automotive body structures, and proficiency in CAD software, often supported by a relevant degree. Experience with tools like CATIA, NX, and familiarity with GD&T standards and manufacturing processes are typically required. Strong problem-solving abilities, teamwork, and effective communication are vital soft skills for collaborating across design, engineering, and manufacturing teams. These skills ensure that vehicle body components are engineered for safety, manufacturability, and cost-effectiveness in a competitive automotive industry.

Design Quality Engineer

Kanak Elite Services Inc

Andover, MA • On-site

Contractor

Posted 10 days ago


Job description

Hello There,
Please go through the below job description and revert me with your Updated Resume and  below details to fasten up the process. 

Email to : yashmita@kanakits.com


Visa-Status :
Location :  
Linkedin Link : 
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ROLE : DESIGN QUALITY ENGINEER

TYPE : ONSITE IN ANDOVER, MA

DURATION : 3-MONTH CTH

INTERVIEW TYPE : VIDEO INTERVIEW

Job Description

As a Design Quality Engineer (DQE) for our medical device manufacturer client in the Greater Boston region, you will be responsible for ensuring end to end design quality and compliance across the product development lifecycle for Class II/III medical devices, including software-driven and active implantable products. Working directly with cross-functional teams, you will drive adherence to design controls, risk management, and SDLC best practices from concept through commercialization and post market activities.

Qualifications:

  • Bachelors degree in Engineering (Biomedical, Software, Systems) or a related technical discipline
  • Advanced degree (Masters) in Engineering, Quality, or Regulatory Affairs preferred
  • Relevant certifications (e.g., ASQ CQE, CSQE, Six Sigma Green/Black Belt) are a plus

Required Skills

  • 10+ years of experience in Quality Engineering supporting regulated medical device development (Class II/III preferred)
  • Strong hands on experience with design controls, DHF management, and traceability in regulated environments
  • Working knowledge of applicable standards and regulations (e.g., 21 CFR 820, ISO 13485, ISO 14971, IEC 62304)
  • Experience supporting software quality within the SDLC and understanding of software risk management principles
  • Proven experience with risk management tools (e.g., FMEA, hazard analysis) and integration into product development
  • Experience supporting audits and regulatory submissions, with the ability to defend design and quality documentation
  • Strong analytical, documentation, and communication skills with ability to work effectively across cross-functional teams
  • Experience with quality systems, eQMS/PLM tools, and defect/CAPA management processes

Key Responsibilities

  • Serving as the quality lead on product development teams, ensuring compliance with design controls across all lifecycle phases (planning, inputs/outputs, verification, validation, transfer, and change management)
  • Establishing and maintaining DHF, DMR, and DHR, ensuring complete traceability from user needs through verification and validation evidence
  • Leading and maintaining risk management activities (hazard analysis, FMEA, risk files) and ensuring integration of risk controls into design and validation activities
  • Providing quality oversight of software SDLC activities, ensuring compliance with applicable standards (e.g., IEC 62304) and integration with system-level risk management
  • Reviewing and approving design, software, and validation deliverables to ensure completeness, consistency, and audit readiness
  • Supporting verification, validation, and design transfer activities, ensuring alignment between design outputs and production processes
  • Leading or supporting CAPA, nonconformance investigations, and root cause analysis to drive continuous improvement
  • Supporting internal and external audits (FDA, Notified Body, ISO), and contributing to regulatory submissions (e.g., IDE, PMA, EU MDR)