Mechanical Engineer

Posted 2 Hours Ago
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Basel, Basel-Stadt, CHE
In-Office
Senior level
Healthtech • Biotech • Nanotechnology • Pharmaceutical
The Role
Develops and industrializes mechanical components, assemblies, prototypes, and medical device technologies from concept through production transfer. Creates CAD models, drawings, requirements, verification tests, and regulatory documentation. Collaborates with software, embedded, manufacturing, and supplier teams; manages design changes and prototype troubleshooting; contributes to project planning; and mentors junior mechanical engineers.
Summary Generated by Built In

About Artidis

Artidis is a pioneering clinical stage health technology company that aims to set the gold standard in tissue analysis and therapy optimization. By combining its nanotechnology platform for rapid tissue analysis with a holistic data solution, Artidis accelerates drug discovery, tissue engineering, and personalized treatment. Artidis focuses its research and development efforts on solid tumors to enhance responses to chemo, immuno, and cell therapies, driving precision in cancer care.

Job Purpose

The Mechanical Engineer provides mechanical engineering expertise for the development, design, and industrialization of Artidis products and technologies. The role independently addresses complex technical challenges from specification and concept development through prototyping, verification, and transfer to production, applying broad expertise in mechanics, manufacturing, and applicable standards. In addition, the Mechanical Engineer serves as a technical reference within the hardware team, supports and mentors junior engineers, and contributes to the planning and coordination of mechanical engineering work packages.

Duties and Responsibilities

  • CAD mechanical part modeling, assembling and drawing, using Autodesk Inventor and Vault (PDM).
  • Create and review detailed technical plans, specifications and layouts for mechanical components and assemblies.
  • Ensure all designs adhere to ISO GPS standards and applicable regulatory/design specifications.
  • Requirements engineering: define technical requirements and design specifications for mechanical parts and assemblies.
  • Collaborate closely with embedded and software engineering teams to integrate mechanical designs with other system components.
  • Design, build and test mechanical prototypes (devices, add-ons, equipment, tools) to validate functionality and design choices.
  • Create design verification tests; develop related test procedures.
  • Lead and contribute to design reviews, providing expert feedback and driving design improvements.
  • Perform necessary modifications and revisions to designs based on feedback.
  • Manage change control of mechanical parts and assemblies through the PDM system.
  • Generate production data and support the transition from development to manufacturing.
  • Communicate and coordinate with suppliers and manufacturers regarding part and assembly production, sourcing and quality issues.
  • Create documentation to be submitted for FDA (US) or Notified Body (EU) approval for medical devices.
  • Ensure the maintenance and troubleshooting of prototypes to keep them operational.
  • Document all design processes, revisions and specifications clearly and accurately.
  • Mentor and provide technical guidance to junior mechanical engineers, including review of their designs.
  • Contribute to project planning for mechanical work packages: define scope, milestones and resource needs, and coordinate timelines with cross-functional teams.

Qualifications

  • Bachelor's or master's degree in Mechanical Engineering or Systems Engineering; specialization in Mechanical Design is an advantage.
  • At least 5 years of professional experience in mechanical design and development, ideally including integrated electro-mechanical systems.
  • Previous experience developing medical devices, with knowledge of regulated processes (ISO 13485 quality management, ISO 14971 risk management).
  • Strong knowledge of ISO GPS.
  • Proven experience with machined parts, welded assemblies, plastic injection and 3D-printed components (plastic and metal).
  • Proficient in Autodesk Inventor and Vault, with the ability to review and validate the work of other engineers.
  • Strong ability to create, review and validate accurate technical drawings and CAD assemblies with attention to detail.
  • Strong knowledge in Design Controls, documentation for FDA or Notified Body submissions.
  • Hands-on experience troubleshooting and maintaining prototypes.
  • Proven problem-solving skills and the ability to investigate and implement efficient mechanical solutions.
  • Demonstrated ability, or clear potential, to mentor and coach junior engineers, providing technical guidance and design review feedback.
  • Some exposure to, or strong interest in, project coordination: planning mechanical work packages, tracking milestones and coordinating with cross-functional teams and external suppliers.
  • Self-initiative, high level of responsibility and strong communication skills.
  • Fluent in English; German is a strong advantage.
Working Conditions

The environment is a typical start-up with an intrinsically motivated international team. Our company is an excellent place for rapid advancement and offers a promising opportunity to learn and share know-how in a very agile environment. The position requires the employee to go the extra mile when needed. We are looking for a team player who appreciates direct communication. The effort is rewarded with challenging tasks, the possibility to take responsibility, a highly driven team, and work serving a significant purpose. The job position comes with a competitive salary and a bonus for outstanding performance.

Skills Required

  • Bachelor’s or master’s degree in Mechanical Engineering or Systems Engineering
  • At least 5 years of professional experience in mechanical design and development
  • Experience developing medical devices and knowledge of regulated processes
  • Knowledge of ISO 13485 quality management
  • Knowledge of ISO 14971 risk management
  • Strong knowledge of ISO GPS
  • Experience with machined parts, welded assemblies, plastic injection, and 3D-printed components
  • Proficiency in Autodesk Inventor and Vault
  • Ability to review and validate other engineers’ work
  • Ability to create, review, and validate technical drawings and CAD assemblies
  • Knowledge of Design Controls and FDA or Notified Body submission documentation
  • Hands-on experience troubleshooting and maintaining prototypes
  • Problem-solving skills and ability to implement mechanical solutions
  • Ability to mentor and coach junior engineers
  • Exposure to or strong interest in project coordination and mechanical work-package planning
  • Self-initiative, responsibility, and strong communication skills
  • Fluent English
  • Specialization in Mechanical Design
  • Experience with integrated electro-mechanical systems
  • German language proficiency
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The Company
HQ: Basel
73 Employees
Year Founded: 2017

What We Do

ARTIDIS AG is a clinical-stage health technology company that aims to set the gold standard in tissue analysis and therapy optimization. By combining its proprietary nanotechnology platform for rapid tissue analysis with a holistic data solution, ARTIDIS accelerates drug discovery, tissue engineering, and personalized treatment. The company focuses its research and development efforts on solid tumors to enhance responses to chemotherapy, immunotherapy, and cell therapies, driving precision in cancer care.

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