| Job alert | Jobs 1 - 10 of 747 |
Quality Assurance Unit Manager I (FDA, GMP, GLP)
SRI International
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Menlo Park, CA
... This is accomplished through proactive inspections and retrospective data / report audits to ensure that all work is conducted in accordance with FDA regulations, international regulations, protocols, Standard Operating Procedures (SOPs), and ... - Jun 19
Embedded Software Manual Test Engineer
Dataverse AI
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Palo Alto, CA, 94306
... 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. ... - Jun 21
Quality Assurance Unit Manager I (FDA, GMP, GLP)
SRI International
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Menlo Park, CA, 94025
... This is accomplished through proactive inspections and retrospective data / report audits to ensure that all work is conducted in accordance with FDA regulations, international regulations, protocols, Standard Operating Procedures (SOPs), and ... - Jun 18
Validation Engineer
Stark Associates LLC
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Newark, CA
... Experience with validation of cGMP automation within FDA-regulated environments. Understanding phases of the Life Cycle Validation approach. Knowledge of GAMP 5, 21 CFR Part 11 and Part 211, EudraLex Volume 4 and Annex 11, and ICH Q7, Q8, Q9, and ... - Jun 17
Eikon Clinical Community
BioSpace
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Hayward, CA, 94557
... In accordance with the Company's duty to provide and maintain a safe workplace, the Company requires all employees to be Fully Vaccinated with one of the FDA approved COVID-19 vaccines, which includes those vaccines that have received the FDA's ... - May 31
Quality Engineer - Hybrid
Cannon Quality Group
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San Jose, CA, 95002
... suppliers and vendors EXPERIENCE REQUIREMENTS: 2+ years of in-depth Quality System implementation in compliance with FDB, FDA, and ISO 13485 2+ years of multiple simultaneous project QA or client facing QA consultancy Experience should include ... - Jun 14
Assembler
CathX Medical
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Sunnyvale, CA, 94088
... This role complies to FDA QSR (21 CFR 820), ISO 13485 requirements and adheres to the Quality Management System (QMS). ESSENTIAL FUNCTIONS: Reads work orders, follows production drawings and sample assemblies, or receives verbal instructions ... - May 23
Assembly Technician II Neurovascular Medical Devices
QAPEL MEDICAL INC
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Fremont, CA, 94538
... Performs daily manufacturing inspection and testing of products to ensure they meet specifications and FDA requirements required. Maintaining legible and accurate records is required. Daily communication with the manufacturing team members, ... - Jun 20
Quality Engineer IV
AbbVie
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Dublin, CA, 94568
... Work in a quality engineering FDA regulated Medical device manufacturing environment. Serve as quality leader on the production line, providing day-to-day oversight & guidance to manufacturing activities. Utilize knowledge of QSR & ISO 13485. Act as ... - Jun 08
Validation Engineer
Stark Associates LLC
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Newark, CA
... Experience with validation of cGMP automation within FDA-regulated environments. Understanding phases of the Life Cycle Validation approach. Knowledge of GAMP 5, 21 CFR Part 11 and Part 211, EudraLex Volume 4 and Annex 11, and ICH Q7, Q8, Q9, and ... - Jun 17