Job Location
Arnoldstein area, Carinthia (Austria)
Company
International Medical Device Company (Anonymized Profile)
Employment Type
Full-time / Permanent
About the Company
Our client is an internationally renowned, innovation-driven pioneer in the field of medical technology. At its modern production and development site in the Arnoldstein (Carinthia) area, highly specialized technological devices are manufactured to set global standards and sustainably improve people's quality of life worldwide. The company is on an ambitious growth path and aims to strategically triple the site's turnover to 30 million euros by the year 2030.
Main Areas of Responsibility - Precision & Accountability
* Incoming Inspection Execution: independent execution and thorough documentation of visual, dimensional, and functional testing on raw materials, complex assemblies, and components according to defined standards.
* Defect Classification: analyzing components and precisely classifying deviations into cosmetic, functional, or safety‑critical defects.
* Supplier Management: monitoring supplier quality, requesting corrective actions, and interacting with international partners in a clear, firm, yet professional and diplomatic manner.
* Technical Validation: checking mechanical connections (e.g., torque specs, thread types, fastener identification) and electrical components (e.g., battery voltage, polarity testing, short circuit recognition).
Technical Qualifications
* Education: Technical diploma, vocational school degree, Master Craftsman (Werkmeister), or Bachelor's degree in Mechanical, Electrical, Industrial Engineering, or Quality Management.
* Technical Skills: Ability to read and fully understand complex technical drawings, solid understanding of mechanical assembly, and basic electrical knowledge (electronics and battery components).
* Regulatory Knowledge: Awareness of quality standards (ISO 9001 base, ideally awareness of or initial exposure to the medical device standard ISO 13485) and standard incoming inspection methodologies.
* Career Changers Welcome: Experience in medical devices is preferred but NOT mandatory. Transferable skills from other highly quality-driven industries such as Automotive, Electronics, Mechatronics, or Semiconductors are explicitly welcome.
Language Requirements (Critical)
* German & English (Mandatory): fluent German and a minimum of B1 English for documentation and international suppliers.
* Italian (A great plus, but NOT mandatory): proficiency in Italian (e.g., B2) is an excellent advantage but not a prerequisite.
Personality Traits
* Detail‑Oriented & Systematic: high precision, structured, leaving nothing to chance regarding quality.
* Persistent & Diplomatic: ability to be firm but professional when enforcing quality requirements internally and externally.
* Self‑Starter with Flexibility: enjoys working independently and comfortable in a dynamic, growing environment even if some processes are still being finalized.
What Is Offered - Your Benefits
* Future & Stability: a crisis‑proof position in a fast‑growing industry worldwide.
* Attractive environment: working in a state‑of‑the‑art facility in the Carinthian border triangle with flat hierarchies and short decision‑making paths.
* Development potential: part of a global corporate group opening excellent, long‑term career advancement opportunities.
* Mobility highlight: attractive commuter arrangements and support options especially for those traveling over 100 km.
Compensation & Framework
For this position, a gross monthly salary starting from €2,700 is offered (based on full‑time employment, 14 salary installments per year). The client offers an explicit willingness to overpay, depending entirely on your individual qualifications and relevant professional experience.
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