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Test Technician/Specialist

Vita Data Sciences
Oberdorf, BL

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Détails de l'emploi

Qualifications

Français
Ingénierie mécanique
Polymécanicien/ne CFC
Anglais
Niveau Master
Niveau Licence
Sens de l'organisation
Compétences en communication
ISO 13485
Allemand

Description complète du poste

Contract: 12 months with possible extension

Location: Oberdorf, Switzerland (On-site mainly with some flexibility)

Our client, a global leader in the medical device industry, is seeking a motivated Test Technician / Test Specialist to join their product testing and verification team in Switzerland. This role offers an exciting opportunity to work hands-on with cutting-edge medical technologies while collaborating closely with experienced engineers in a highly regulated environment.

Ideal for professionals looking to advance in roles such as Product Test Engineer, Verification & Validation (V&V) Engineer, or Mechanical Test Engineer, this position provides exposure to innovative testing methods, ISO/FDA compliance, and product lifecycle development.

Key Responsibilities

Plan, coordinate, prepare, and execute recurring mechanical product tests in collaboration with Senior Test Engineers.
Conduct routine and complex testing activities independently, ensuring accuracy and adherence to SOPs, ISO, and FDA requirements.
Evaluate and interpret test results, prepare test protocols, reports, and enter data into IT/LIMS systems.
Support the development and validation of new test methods and contribute to the creation of standard operating procedures (SOPs).
Maintain and update test instructions and documentation within the document management system.
Collaborate effectively with internal and external clients to meet testing deliverables and timelines.
Ensure full regulatory compliance and participate in continuous improvement initiatives to optimize testing efficiency.

Profile & Qualifications

Completed apprenticeship (e.g., Polymechanic, Laboratory Technician) with 1–2 years of experience in product testing or
a Bachelor’s/Master’s degree in Biomedical Engineering, Mechanical Engineering, or related field.
Prior experience in product testing, verification & validation, or medical device testing strongly preferred.
Knowledge of ISO 13485, ISO 14155, or FDA 21 CFR Part 820 is a strong plus.
Strong organizational skills, attention to detail, and initiative.
Excellent written and verbal communication skills (English required; German or French an advantage).
Proactive team player with a hands-on attitude and the ability to adapt in a dynamic environment.

What’s Offered

Opportunity to work for a global leader in medical technology, with exposure to high-impact products.
Full benefits and competitive remuneration package.
Professional development and hands-on training in product verification, validation, and testing.
Collaborative and innovative team environment.

Soumettre votre candidature

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Je souhaite recevoir la dernière alerte Emploi pour les postes de ce type : specialist (niederbipp, be)

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