Electrical Engineer, Oberdorf

Location: Oberdorf, Switzerland (German or French speaking preferred)

Responsibilities

Lead and support

New Product Introduction (NPI)

activities in a regulated medical device environment

Author and execute

validation protocols (IQ / OQ / PQ)

and ensure compliance with quality standards

Collaborate closely with

R&D, quality, manufacturing, and regulatory teams

Support

design transfer

from development to manufacturing

Drive

CAPA investigations, root cause analysis, and risk management activities

Participate in

PCB design reviews and collaboration with electronics teams (Altium environment)

Ensure compliance with

ISO 13485, MDR, and other regulatory requirements

Contribute to

process improvements and continuous quality initiatives

Qualifications

Strong experience in

Medical Device / MedTech regulatory environments

Hands‑on experience with

validation activities (IQ / OQ / PQ)

Experience with

CAPA, risk management, FMEA, and SPC

Exposure to

ISO 13485 and MDR regulatory frameworks

Experience supporting

design transfer and product industrialization

Knowledge of

PCB development and collaboration using Altium tools

Strong

engineering background

German or French is highly preferred

Experience with

end‑to‑end NPI programs in regulated environments

Proven ability to work in

cross‑functional international teams

If you are interested in learning more, feel free to

apply or reach out directly via LinkedIn .

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