**The main purpose of this**role **is to perform semi-standardized or semi-prescribed tasks that require judgment and problem-solving skills. Responsible for updating and reviewing procedures or standard equipment.**
**The position is also responsible for monitoring of compliance with cleanroom requirements during production and ensures product quality for dimensional, electrical and visual workmanship standards according to customer requirements.**
**ROLES AND RESPONSIBILITIES**
- Closely monitors daily, weekly and monthly quality indicators and metrics.
- Identifies and evaluates procedures to ensure the manufacturing aligned with our quality standards.
- Validates product specifications using measurement tools and techniques.
- Conducts studies to understand the capability of process and/or measurement systems.
- Provides technical support as required by the quality team and other areas.
- Performs the final review of the Manufacturing Device History Record (DHR) at the end of the manufacturing process and product launch.
- Makes decisions about how to handle product issues with the operator accordingly and issues related to whether the product is acceptable or not.
- Prepares technical reports, standards and rejection records, and other required quality documentation.
- Sets up and run experiments and/or test devices with steering.
- Provides inputs in the evaluation of equipment and processes.
- Demonstrates safe work habits, maintains a clean and safe work area.
**Requirements**:
- Technical degree and or advanced university studies in the areas of engineering, quality, Life Sciences is required.
- At least 3 years of experience in the medical industry or highly regulated industry is required.
- Intermediate or advanced verbal and written English language skills.
- Knowledge in Metrology.
- Desirable knowledge in equipment calibration.
**Benefits**
Market competitive package