Quality Assurance Specialist
Altatec(2 days ago)
About this role
This role involves supporting quality assurance activities for medical devices, ensuring compliance with regulatory standards such as ISO 13485, and participating in document control and training activities. It requires collaboration within the organization to maintain quality standards and support regulatory requirements.
Required Skills
- ISO 13485
- Regulatory Compliance
- Documentation
- Quality Assurance
- CAPA
- FDA Regulations
- ISO Standards
- Medical Devices
- Quality Management
- Auditing
About Altatec
altatec.chAltatec Microtechnologies AG is an innovative small and medium-sized enterprise (SME) located in the heart of Switzerland, specializing in the development and production of products in the field of microtechnology. The company focuses on creating high-quality microelectronics solutions tailored to meet the needs of its clients. With a commitment to innovation, Altatec positions itself as a key player in the microtechnology sector, offering advanced solutions that leverage cutting-edge technology.
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