As a Quality Assurance Manager in a medical device factory, your primary responsibility is to ensure that all products meet or exceed quality standards and regulatory requirements. You will be responsible for developing and implementing quality management systems, leading quality improvement initiatives, and overseeing the entire Quality Assurance process. Your role is crucial in maintaining the safety, efficacy, and reliability of medical devices produced in the factory.
Requirements: Bachelor's degree in engineering, life sciences, or a related field. A master's degree is a plus
- Extensive experience (typically 5+ years) in Quality Assurance, preferably in the medical device industry.
- In-depth knowledge of quality management systems,, and relevant industry standards.
- Strong understanding of manufacturing processes, quality control methods, and statistical techniques.
- Experience in leading cross-functional teams and implementing quality improvement initiatives.
- Excellent problem-solving skills and the ability to conduct root cause analysis and implement corrective actions.
- Strong organizational and project management skills, with the ability to prioritize and manage multiple tasks simultaneously.
- Excellent communication skills, both written and verbal, with the ability to effectively communicate with employees at all levels of the organization.
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