Beschreibung
Quality Manager/Analyst - Medical Devices - Zug
Our client is a leader within the medical devices industry. They are seeking an experienced consultant who is able to perform a number of duties around Quality Management.
Key Responsibilities
Production and test environment:
- Creation and maintenance of the specification and the supporting documents for the manufacture of products
- Creation and maintenance of the work plans, the material master data and BOMs
- Technically supervision of staff with technical problems exhibit
- Training of default and the supporting documents for the manufacture of products
Verification/Validation/Qualification:
- Support for the professional examination of the documents
- operation and aids defining including modifying, and/or procure
Variations in process and result in faulty test:
- Support of regular analysis and data reviews
- Implementing improvements derived from the analysis and data evaluation
Fault Management:
- Identify causes and/or start communication with supplier
- Provide correct procure material
- Define corrective measures agreed with Technical Supplier Management and reacted with Supplier
- Review and conclusion based on existing process
Requirements
* Technical Background
* Experience in highly regulated GxP environment of medical devices
* Experience, for example, as quality manager, or similar activities in quality assurance of benefit
* Laboratory experience is an advantage
Computer Skills
* SAP
* MS Office
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Languages spoken and written :
* German
* English