| Job alert | Jobs 51 - 60 of 746 |
Software Verification Engineer (Medical Device)
Intellectt INC
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Palo Alto, CA
... Ensure testing complies with regulatory standards (FDA, ISO 13485, IEC 62304). Stay updated with industry best practices and regulatory requirements. Qualifications: Bachelor's degree in Computer Science, Software Engineering, Biomedical Engineering ... - Jun 19
Principal R&D Engineer, Preclinical
Imperative Care
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Campbell, CA, 95008
176000-191000 per year
... and data collection Extensive experience working under quality systems designed to meet governmental regulations such as FDA QSR, ISO 13485, and the MDD Extensive experience in full R&D product life cycleEmployee Benefits include a stake in our ... - Jun 05
Software Verification Engineer (Clinical)
Intellectt INC
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Palo Alto, CA
... Compliance and Standards Ensure testing activities comply with relevant regulatory standards (e.g., FDA, ISO 13485, IEC 62304). Stay updated with industry best practices and evolving regulatory requirements for medical device software. Education: ... - Jun 17
Senior Software Engineer
Neuralink
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Fremont, CA, 94537
... that place a strong emphasis on high-precision and high-repeatability mechanical motion, high reliability, and fail-safe design Design and ship software for brain surgical robots in compliance with the Food and Drug Administration (FDA). ... - Jun 08
Clinical Trial Associate, Oncology, EMEA
BioSpace, Inc.
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Hayward, CA, 94557
... or CRO industry is preferred Knowledge of clinical trial regulations, guidelines, and best practices, including ICH-GCP and FDA requirements Strong organizational skills and attention to detail, with the ability to manage multiple tasks and ... - Jun 22
Director of Manufacturing Engineering
The Mullings Group
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Menlo Park, CA
... This person should demonstrate a deep understanding of FDA regulations, specifically for Class II IVD products, and will be proficient in ISO 13485 standards for medical devices. Key Responsibilities: Serve as primary engineering contact for ... - May 31
Med-Tech Media Marketing Specialist
Zeto, Inc
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Santa Clara, CA
... Devise media mrktng strategies for FDA-cleared med devices for media & public - Jun 11
Director of Regulatory Affairs
Mastech Digital
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Pleasanton, CA, 94566
... In addition, this position leads CTP in a comprehensive knowledge of FDA, GCP, GDPR regulations and ICH E6 R2 guidelines. This position reports to the Managing Director, Clinical Trials Program. Primary Duties and Responsibilities: ● Providing ... - May 26
Quality Engineer
Unigen Corporation
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Newark, CA
... Certify or experience in any of IATF, Automotive 5 Core-tools, ISO13485, FDA, ISO14001, ISO9001, or Six Sigma Green or Black Belt certification is strongly preferred. Salary Range: $80K- $130K/ year Company Description Originally established in 1991 ... - Jun 08
Complaint Coordinator
GTT, LLC
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Livermore, CA, 94550
... Demonstrates thorough understanding of quality management standards as outlined in Good Manufacturing Practices (GMPs), FDA Code of Federal Regulations (CFRs), and ISO 13485. Actively participates in departmental process improvements and effectively ... - Jun 21