Professional Summary
Professional Overview
Tamir Shefer is an experienced Regulatory Affairs (RA) and Quality Assurance (QA) Consultant with a strong background in the medical devices industry. He specializes in ensuring regulatory compliance, implementing quality management systems, and driving continuous improvement initiatives to enhance product safety and efficacy.
Experience Summary
Current Role
Tamir currently serves as an RA & QA Consultant at Medical Devices, where he leverages his expertise to support clients in navigating complex regulatory landscapes and optimizing their quality assurance processes. In this role, he collaborates closely with cross-functional teams to develop and implement strategies that align with industry standards and best practices.
Career Progression
Prior to his current position, Tamir held various leadership roles in the field of quality assurance and regulatory affairs. He served as the Director of Quality Assurance and Regulatory Affairs at Nanopass Technologies Ltd., where he was responsible for establishing and maintaining robust quality management systems. Before that, he held the role of Director of Quality Assurance at Nanopass Technologies Ltd., overseeing the company's quality initiatives and driving continuous improvement.
Tamir's career also includes experience at renowned organizations such as Philips Healthcare, Cheetah Medical, BioControl Medical, Initia Ltd., Medisim Ltd., Tessera (Former ShellCase), and Biometrix, where he consistently demonstrated his ability to navigate complex regulatory landscapes and ensure the delivery of high-quality medical products.
Academic Background
Tamir holds a relevant educational background, though specific details are not provided in the given information.
Areas of Expertise
- Regulatory affairs and compliance
- Quality assurance and quality management systems
- Medical device industry standards and regulations
- Continuous improvement and process optimization
- Cross-functional collaboration and stakeholder management
Professional Impact
Throughout his career, Tamir has made valuable contributions to the medical devices industry. His expertise in navigating regulatory requirements and implementing robust quality assurance practices has enabled his employer organizations to maintain compliance, optimize product quality, and drive operational efficiency.
Conclusion
With his extensive experience, deep industry knowledge, and proven track record of success, Tamir Shefer is a highly skilled RA and QA Consultant who is well-equipped to support organizations in the medical devices sector. His unwavering commitment to quality and regulatory compliance, coupled with his strategic problem-solving abilities, make him a valuable asset in the industry.
