22 Medical Devices Regulatory Jobs in Pune - page 2
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Software Technologist I - Embedded C++ Pune, India , etc. Experience in software development in medical industry or highly regulated industry. Experience with IEC 62304, FDA guidance for medical device development and other relevant medical device Not Mentioned More than 30 days ago
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Software Technologist I/II - Embedded Pune, India . Experience in software development in medical industry or highly regulated industry. Experience with IEC 62304, FDA guidance for medical device development and other relevant medical device regulatory Not Mentioned More than 30 days ago
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DESIGN QUALITY ASSURANCE Pune, India . Sound understanding of medical device regulatory requirements for Class II and III medical devices. Project planning resourcing, timelines, quality and budgets. Skilled in implementing Quality tools like Not Mentioned 16 days ago
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Regulatory Specialist Pune, India with relevant medical device standards, codes and regulations. S/he provides medical device regulatory input to product labeling, including but not limited to product labels, Instructions for Use (IFUs), surgical Not Mentioned 8 days ago
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Systems Engineer Pune, India Verification and Validation plan/protocols, Test Method Validation (TMV) Conducting Technical Review & Decision Making Understanding of global medical device regulatory environments and clearance processes Not Mentioned 5 days ago
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QT/QML Specialist Pune, India Tata Elxsi works with leading medical device OEMs and technology companies for market research and human factor engineering, hardware and software engineering, verification & validation, regulatory Not Mentioned More than 30 days ago
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Systems Engineer Pune, India and Validation) activities, generating, and analyzing test reportsu00A0 Understanding of global medical device regulatory environments and clearance processes.u00A0 Effective communication, computer, documentation Not Mentioned 25 days ago
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System Test Architect (System V&V) - Medical Devices Pune, India + yearsu2019 experience with Minimum 5 years of experience in medical device or other similar industry Demonstrated knowledge of global quality and regulatory environment for medical devices including FDA CFR 21 Not Mentioned 3 days ago
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Associate Director Regulatory Affairs MoS Pune, India discipline(s) Minimum of 15+ years' experience working in Regulatory Affairs within medical device/technology environments, with 8+ years' as a functional leader and strong track-record successfully leading Not Mentioned 20 days ago
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Quality System Manager Pune, India medical device design development quality systems to satisfy international requirements and global regulatory needs. Major Responsibilities Include, But Not Limited To Lead establish and maintain quality Not Mentioned More than 30 days ago
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