Mechanical Engineer II, Medical

Goddard

San Diego (CA)

On-site

USD 80,000 - 100,000

Full time

14 days+

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Benefits offered by this job

Flexible Time Off
401(k) retirement plan
Health coverage
Parental leave
Company events

Job summary

Goddard in San Diego, CA is seeking a Mechanical Engineer II with 3–5 years of experience in medical devices, product development, and mechanical design. You’ll join a team of engineers executing projects with on-time deliverables in a hands-on role.

Expect 3–4 days per week in the office at either the San Diego site or a client location. Proficiency in SolidWorks and PDM is required; strong collaboration across disciplines is essential.

Qualifications

  • Bachelor’s degree in mechanical engineering or related field is required.
  • Hands-on medical device development and design experience preferred.
  • Familiarity with FDA design controls and ISO 13485/14971 standards.

Responsibilities

  • Develop mechanical concepts for packaging strategies and components.
  • Create models in SolidWorks and work within PDM systems.
  • Design verification testing plans and collaborate with cross-functional teams.
  • Support lab studies, root-cause analyses, and tolerance analyses.
  • Ensure designs meet budget, schedule, and quality requirements.
  • Communicate project risks and engage in problem resolution.

Skills

Medical device manufacturing
FDA design controls
Drafting (2D/GD&T)
Team collaboration
Problem solving

Education

Bachelor's degree in mechanical engineering

Tools

SolidWorks
PDM

Job description

Our Mission

Through inspired engineering and design, we deliver outstanding solutions that positively impact lives. We use an interdisciplinary development process that combines our diverse engineering experience with creative industrial design solutions. We succeed when our partners succeed – it’s all about solving the most complex challenges by creating transformative technology.

Our Culture And People

At Goddard, our most important asset is our people. We don't just work together; we thrive together. We foster a culture of collaboration, continuous learning, and mutual support. We believe in taking exceptionally good care of each other because great teams build great solutions. If you are someone who embodies the values of accountability, inspiration, dedication, efficiency, innovation, integrity, quality, and reliability, we want you on our team. Come be a part of a workplace where your ideas are valued, your growth is encouraged, and your contributions make a real impact. Join us in shaping the future of transformative technology – together.

The Role

The Mechanical Engineer II will have 3-5 years of experience in medical devices, product development, mechanical design, and engineering. This role will be part of a team of engineers to execute projects, ensuring on-time submission of deliverables. This is a hands‑on position that will require, on average, 3-4 days per week in office (either in SD office or a local client site).

Responsibilities
  • Eager to learn, build, try things, fail, improve, and repeat
  • Build prototypes and iterate quickly to derisk design direction
  • Ability to track to a budget. Knowing “what good looks like” and when to stop iterating to conserve client funds
  • Plan and execute lab notebook studies, pre-verification studies, and design verification testing. Get buy in from cross‑functional groups with conflicting priorities
  • Create models in Solidworks and work within the Goddard or client PDM
  • Contribute to client interactions with clear communication to deliverables, design reviews and deadlines
  • Work independently or as part of a team to create mechanical concepts for overall packaging strategies, mechanisms, and parts while balancing function, appearance, form, and budgetary requirements
  • Provide DFX expertise to ensure designs are optimized
  • Support or design and develop precision mechanical products utilizing injection molding plastics, machining, casting, laser cutting and welding, extrusion and 3D printing
  • Execute iterative development cycles using rapid prototyping, root cause analysis, tolerance stack analysis, FEA, concept down‑selection tools, or other engineering methods
  • Create or assist in Document Design History File development activities including but not limited to Design and Development planning, system requirements, RISK management, hazard analysis, xFMEA, design inputs and outputs, test plans, protocols and reports
  • Work with team members to resolve technical conflicts between clients and engineering teams
  • Support prioritization and design decisions between interdisciplinary team members including electrical engineers, software engineers, human factors engineers, systems engineers and industrial designers
  • Operate within a Quality Management System as well as contribute to continuous improvement effortsRemain apprised of the progress of certain projects, paying particular attention to any developing problems, and participate in major problem resolutions
  • Communicate to management any significant project risks, deviations from plans and proposed solutions to course correct
  • Travel as needed (valid driver’s license and vehicle required)
  • Keep all privileged information private and confidential
Qualifications
  • Positive attitude, hunger to learn and grow
  • Bachelor’s degree in mechanical engineering or related field
  • Proven experience in one or more of the following industry segments: Neurology, Cardiovascular, Orthopedics, Women’s Health, and Diabetes
  • Hands on medical device test experience
  • Functional knowledge of FDA design controls 21 CFR Part 820 and recognized standards such as ISO 13485 and 14971 and IEC 60601
  • Proficiency in SolidWorks CAD package and PDM
  • Working knowledge of common sterilization methodologies, biocompatibility, sterile packaging, shelf‑life, and simulated distribution validation testing
  • 2D drawing creation, GD&T, tolerance analysis
  • Strong teamwork, interpersonal and communication skills, and a demonstrated ability to work at a high level of performance both independently and collaboratively
  • Hands‑On medical device manufacturing experience
Our Benefits
Flexible Time Off

Benefit from our generous flexible time off policy. We also provide sick leave and bereavement time because we understand that not all time off is for fun.

Retirement Savings

Invest in your future with a 401(k) retirement plan. Goddard contributes 3% of your annual salary directly into your 401(k) account—regardless of your own contributions.

Health Coverage

Access to comprehensive medical, dental, and vision insurance for you and your family. Goddard contributes 80% of monthly premiums for all medical plan options.

Family Support

To take the time you need to welcome the newest member of your family, Goddard offers 6 weeks fully paid parental leave with support of PFML state programs.

Company Engagement

Engage with your colleagues through a variety of regular company and team events, including weekly social hours, Athletic Club outings, and department outings.

Pay Range For This Role Is

80,000 - 100,000 USD per year (San Diego, CA)

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