Device Quality
1 week ago
Our vision is to transform how the world uses information to enrich life for all.
Micron Technology is a world leader in innovating memory and storage solutions that accelerate the transformation of information into intelligence, inspiring the world to learn, communicate and advance faster than ever.
As a key technical member of the Develop Design Quality Assurance (DDQA) NAND team, you will work collaboratively with our technology development, design and test engineering teams to predict and solve product failure modes. Your role will be pivotal in building reliability models and consulting with both the device development and circuit design teams. Additionally, you will work closely with media health and test solution engineers to develop fault isolation strategies and create new risk assessment methods. This work requires a solid understanding of semiconductor device physics and NAND architecture.
Your responsibilities will include
Implement technical risk assessment and NUDD (New, Unique, Different, Difficult) analysis when new designs, circuit, device, layout and process and lead execution of risk mitigation Developing and implementing test methodologies to evaluate wafer-level and circuit-level PRODUCT reliability behavior and performance. Collaboration with technology development, design, reliability, and characterization teams will be essential for reliability model building signatures with process conversions and parametric test data. Integrate data sources (metrology, param, product test) to model physical fail modes and providing actionable recommendations for develop quality and reliability mitigation strategies in product design, development and test will be key aspects of your role.Qualifications:
A solid understanding of semiconductor device physics and circuit operation. Basic knowledge of NAND memory and semiconductor process technology Proficiency in statistical data analysis. Exceptional communication skills are essential, along with 3 to 8 years of experience in the semiconductor industry or a research institute. Expertise in semiconductor device parametric measurement and proficiency in operating semiconductor lab instrumentation for electrical characterization are highly valued. Good understanding of Advanced CMOS Device Engineering and NAND integration. Educational qualifications include an or in Electrical Engineering, Physics, Materials Science, or a related field with at least 2 years of experience.-
Device Quality
3 weeks ago
Hyderabad, India Micron Technology Full timeOur vision is to transform how the world uses information to enrich life forall .Micron Technology is a world leader in innovating memory and storage solutions that accelerate the transformation of information into intelligence, inspiring the world to learn, communicate and advance faster than ever. As a key technical member of the Develop Design Quality...
-
Device Quality
6 days ago
Hyderabad, Telangana, India Micron Technology Full time ₹ 7,00,000 - ₹ 12,00,000 per yearOur vision is to transform how the world uses information to enrich life forall.Micron Technology is a world leader in innovating memory and storage solutions that accelerate the transformation of information into intelligence, inspiring the world to learn, communicate and advance faster than ever.As a key technical member of the Develop Design Quality...
-
Regulatory lead, medical devices
2 days ago
Hyderabad, India ArtiXio Full timeAbout the Role We are looking for a Medical Device Regulatory Lead with 4–6 years of proven hands-on experience in medical device regulatory submissions and compliance. The ideal candidate will have strong expertise in preparing and submitting applications to Health Authorities including US FDA (510k), Europe (CE Marking), MDSAP, CDSCO , and other global...
-
Regulatory Lead, Medical Devices
2 weeks ago
Hyderabad, India ArtiXio Full timeAbout the Role We are looking for a Medical Device Regulatory Lead with 4–6 years of proven hands-on experience in medical device regulatory submissions and compliance. The ideal candidate will have strong expertise in preparing and submitting applications to Health Authorities including US FDA (510k), Europe (CE Marking), MDSAP, CDSCO , and other...
-
Medical Device Regulatory Lead
5 days ago
Hyderabad, India ArtiXio Full timeAbout the RoleWe are looking for a Medical Device Regulatory Lead with 4–6 years of proven hands-on experience in medical device regulatory submissions and compliance. The ideal candidate will have strong expertise in preparing and submitting applications to Health Authorities including US FDA (510k), Europe (CE Marking), MDSAP, CDSCO, and other global...
-
Medical device regulatory lead
2 weeks ago
Hyderabad, India ArtiXio Full timeAbout the Role We are looking for a Medical Device Regulatory Lead with 4–6 years of proven hands-on experience in medical device regulatory submissions and compliance. The ideal candidate will have strong expertise in preparing and submitting applications to Health Authorities including US FDA (510k), Europe (CE Marking), MDSAP, CDSCO , and other...
-
Medical device regulatory lead
3 days ago
Hyderabad, India ArtiXio Full timeAbout the RoleWe are looking for a Medical Device Regulatory Lead with 4–6 years of proven hands-on experience in medical device regulatory submissions and compliance. The ideal candidate will have strong expertise in preparing and submitting applications to Health Authorities including US FDA (510k), Europe (CE Marking), MDSAP, CDSCO , and other global...
-
Medical device regulatory lead
3 days ago
Hyderabad, India ArtiXio Full timeAbout the RoleWe are looking for a Medical Device Regulatory Lead with 4–6 years of proven hands-on experience in medical device regulatory submissions and compliance. The ideal candidate will have strong expertise in preparing and submitting applications to Health Authorities including US FDA (510k), Europe (CE Marking), MDSAP, CDSCO , and other global...
-
Medical Device Regulatory Lead
2 weeks ago
Hyderabad, India ArtiXio Full timeAbout the RoleWe are looking for a Medical Device Regulatory Lead with 4–6 years of proven hands-on experience in medical device regulatory submissions and compliance. The ideal candidate will have strong expertise in preparing and submitting applications to Health Authorities including US FDA (510k), Europe (CE Marking), MDSAP, CDSCO , and other...
-
Medical Device Regulatory Lead
1 week ago
Hyderabad, India ArtiXio Full timeAbout the RoleWe are looking for a Medical Device Regulatory Lead with 4–6 years of proven hands-on experience in medical device regulatory submissions and compliance. The ideal candidate will have strong expertise in preparing and submitting applications to Health Authorities including US FDA (510k), Europe (CE Marking), MDSAP, CDSCO, and other global...
