Description
Job Summary:
This position supports the operational activities of the Regional Quality Coordinator by performing quality inspection, sampling, and documentation for medical devices.
Key Highlights:
1. Supports quality inspection and sampling of medical devices
2. Identifies and documents quality deviations
3. Supports continuous improvement of the quality system
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**Job Description:**
**Description**
This position supports the operational activities of the Regional Quality Coordinator.
**Responsibilities:**
* Supports the Regional Quality Coordinator in attribute-based inspection and sampling of medical devices (disposable products).
* Supports the Regional Quality Coordinator in attribute-based inspection and sampling of products exiting the conditioning process and documents such activities in the relevant records.
* Identifies and submits photographic evidence of deviations affecting the quality of medical devices across various processes (Receiving, Inspection, Conditioning, and Storage) to the Regional Quality Coordinator and/or Technical Management.
* Reports all deviations occurring during processes (Receiving, Inspection, Conditioning, and Storage) to the Regional Quality Coordinator and/or Technical Management.
* Enters import and return data into databases in real time.
* Accompanies inspections conducted by the Regional Quality Coordinator and/or Technical Management during self-inspection visits or as otherwise required.
* Verifies that non-conforming product segregation processes are performed per customer guidelines.
* Performs verification of conditioned products.
* Reviews operational records (temperature, cleaning, and sanitation).
* Supports quality inspections of operational processes.
* Supports Good Manufacturing Practice (GMP) training.
* Supports maintenance and determination of necessary actions to continuously maintain and improve the company’s quality management system.
* Verifies that measurement or calibration equipment in the area is maintained in good condition.
* Knows and applies procedures, work instructions, and forms related to performed operations.
**Requirements:**
* Technical background: Quality Control, Document Management, Quality Control, Quality Management, Integrated Management Systems, Management System Auditing, Industrial Processes, Corporate Logistics
* Desired experience: 1–2 years
* Work location: Siberia
* Employment type: 100% on-site
* Schedule: Monday to Friday (Saturday availability required if operationally necessary)
**Employee Type:**
Permanent
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