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Temporary Manufacturing & Quality Control Assistant

Artidis
Basel, BS, Switzerland Posted Nov 6, 2026
Full-timeOn-site

About this role

Temporary Manufacturing & Quality Control Assistant

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.

Start Date: As soon as possible Employment Type: Fixed-term temporary position Duration & Workload: 3 months at 100% or 6 months at 40–50%

Duties and Responsibilities

  • Perform non-destructive quality inspections of AFM probes, including 100% inspection of designated batches.
  • Accurately document inspection results and report quality deviations.
  • Support improvements to testing protocols and inspection methods.
  • Operate and optimise a small 3D printer farm producing packaging components for disposables.
  • Inspect printed parts and perform post-processing or rework as required.
  • Maintain and improve manufacturing documentation.
  • Support R&D with prototype production.

Qualifications

  • Technical background or practical experience in manufacturing, engineering, quality inspection or a related field.

  • Strong attention to detail and ability to perform repetitive inspection tasks accurately and consistently.

  • Hands-on mentality and a structured, reliable working approach.

  • Ability to work independently and follow established procedures.

  • Experience with 3D printing or quality control is an advantage but not required.

  • Students and individuals seeking temporary employment are welcome to apply.

  • Working Conditions

  • A flexible, fixed-term opportunity: 3 months full-time or 6 months part-time (40–50%).

  • Practical experience in an innovative medtech environment.

  • Hands-on responsibilities in manufacturing and quality inspection.

  • A collaborative and international team.

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