Test Technician/Test Specialist (Medical Devices) Join to apply for the
Test Technician/Test Specialist (Medical Devices)
role at
Kelly Science, Engineering, Technology & Telecom
Contract duration: 12 months with possible extension
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.
Seniority level Entry level
Employment type Full‑time
Job function Science
Industries Medical Equipment Manufacturing
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