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Samin Eftekhari, EIT., PhD.
Biomedical Engineer (Biomaterials), Lung Biotechnology PBC, United Therapeutics at United Therapeutics
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Samin Eftekhari, EIT., PhD.
Biomedical Engineer (Biomaterials), Lung Biotechnology PBC, United Therapeutics at United Therapeutics
Joined 01/12/2018
Level: LEVEL 01 (12 mo pts: 0 pts)
Lifetime points: 0 pts
Samin Eftekhari is a biomaterial scientist, researcher, Inventor, and entrepreneur. Samin has more than 10 years of experience in multi-disciplinary engineering including Materials Science, Biomedical, and Chemical Engineering.
SUMMARY OF QUALIFICATIONS
• Strong knowledge of Materials Science, Biomedical Science, and Chemical Engineering
• Experienced in creation and testing of the prototypes
• Experienced in characterization techniques of metals, polymers, ceramics, and their composites
• Proficiency in Design of Experiments (DOE) and statistical analysis
• Ability to write clear and accurate descriptions of pre-clinical studies and bench-top
• Working knowledge of biocompatibility test according to ISO 10993
• Working knowledge of developing medical devices according to ISO 13485 & 21 CFR 820
• Experienced in FDA Regulatory Submissions such as Q-Subs, 510 (K), and PMAs
• Working Knowledge of mechanical testing, thermal analysis,
• Over 5 years of experience in R&D activities for New Product Introducing (NPI) and testing
• Experienced in intellectual property development and patent application writing
• Expertise in development of technical and commercial grant proposals
• Experienced in successful leadership, project planning, and project management
• Highly skilled in time-management, and prioritizing the deliverable based on deadlines
SUMMARY OF QUALIFICATIONS
• Strong knowledge of Materials Science, Biomedical Science, and Chemical Engineering
• Experienced in creation and testing of the prototypes
• Experienced in characterization techniques of metals, polymers, ceramics, and their composites
• Proficiency in Design of Experiments (DOE) and statistical analysis
• Ability to write clear and accurate descriptions of pre-clinical studies and bench-top
• Working knowledge of biocompatibility test according to ISO 10993
• Working knowledge of developing medical devices according to ISO 13485 & 21 CFR 820
• Experienced in FDA Regulatory Submissions such as Q-Subs, 510 (K), and PMAs
• Working Knowledge of mechanical testing, thermal analysis,
• Over 5 years of experience in R&D activities for New Product Introducing (NPI) and testing
• Experienced in intellectual property development and patent application writing
• Expertise in development of technical and commercial grant proposals
• Experienced in successful leadership, project planning, and project management
• Highly skilled in time-management, and prioritizing the deliverable based on deadlines
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