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Senior Mechanical Engineer, Medical

Job in Beverly, Essex County, Massachusetts, 01915, USA
Listing for: Goddard Technologies, Inc.
Full Time position
Listed on 2026-04-29
Job specializations:
  • Engineering
    Mechanical Engineer
Salary/Wage Range or Industry Benchmark: 100000 - 125000 USD Yearly USD 100000.00 125000.00 YEAR
Job Description & How to Apply Below

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 Senior Mechanical Engineer will have5+ years of experience in medical devices, product development, mechanical design, and engineering. This role will lead, advise, and assist a team of engineers to execute projects, ensuring on-time submission of deliverables.

Responsibilities
  • Manage and facilitate client interactions with clear communication as it relates to deliverables, design reviews and deadlines.
  • Work independently, as a team leader 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.
  • 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.
  • Lead and 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.
  • Plan and execute formal verification testing, including test method development, test method validation, data analysis, and design of experiments.
  • Work with team members to resolve conflicts among resources and between clients and engineering teams.
  • Coordinate priorities 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 efforts.
  • Remain apprised of the progress of certain projects, paying particular attention to any developing problems, and participate in major problem resolutions.
  • Support project scoping activities to support Business Development and Sales teams.
  • Communicate to senior management any significant project risks or deviations from the plans.
  • Serve as a mentor for less experienced team members.
  • Travel as needed (valid driver’s license and vehicle required).
  • Keep all privileged information private and confidential.
Qualifications
  • 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.
  • A functional knowledge of FDA design controls 21 CFR Part 820 and recognized standards such as ISO 13485 and 14971 and IEC 60601.
  • Proficiency in the latest version of Solid Works CAD package.
  • 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.
Our Benefits

Flexible Time Off:

Position Requirements
10+ Years work experience
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