- Maintaining and further developing quality management system in accordance with ISO 13485, which includes.
- Documentation management
- Auditing
- Training courses
- Error detection and correction
- Risk Management
- Life Science or Engineering academic background
- Professional experience in a regulated environment is an advantage, ideally in the quality sector a preferred would be medical technology.
- Extensive knowledge of ISO 13485 and MDR regulatory standards.
- Knowledge of the relevant quality standards and technical norms.
- Very good verbal and written communication skills in English and German
- IT user skills (Word, Excel, Outlook) with experience in using electronic document management software as an advantage
- A high degree of teamwork and communication skills
- Independent, structured and results-orientated working style
- Professional experience in quality management and auditing in a medical device environment.
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Quality Management Specialist - Munich Metropolitan Area, Deutschland - PROJECTUS
vor 3 Tagen
Beschreibung
QUALITY MANAGEMENT SPECIALIST
OVERVIEW:
As the ISO 13485 Quality Specialist you will play a critical role in ensuring compliance with quality management standards. You will oversee the development, implementation and maintenance of our quality management system and ensure compliance with the regulatory requirements.
KEY ACCOUNTABILITIES:
SKILLS/EXPERIENCE REQUIRED:
Due to the high amount of applications, if you do not hear back from Project Consulting in 7 days please assume your application has been unsuccessful on this occasion.
