| Job alert | Jobs 31 - 40 of 753 |
Director Quality Regulatory Affairs
Insight Global
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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 ... - Jun 02
Director, CMC Regulatory
Revolution Medicines, Inc.
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Redwood City, CA, 94063
... * Participate in the interactions with FDA and other global regulatory authorities as appropriate. * Provide regulatory assessment and guidance on CMC-related change controls, deviations, and investigations throughout the product life cycle. * ... - May 24
Complaint Coordinator
Intellectt INC
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Livermore, CA
... 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 19
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 19
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 ... - Jun 17
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
Production - General Support
National Beverage
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Hayward, CA, 94557
... Must follow the work rules at all times as given in the Employee Handbook entitled, "Welcome to National BevPak." GMP (Good Manufacturing Practices) and FDA (Food and Drug Administration) compliance MUST be adhered to at all times. Keep the work ... - Jun 06
Senior Quality Specialist
Kelly Science, Engineering, Technology & Telecom
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Sunnyvale, CA, 94087
... Quality Specialist is responsible for supporting quality systems activities related to assay development, especially, design control and risk management activities in accordance with FDA and ISO regulations. This position is part of the Product ... - Jun 18
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
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