| Job alert | Jobs 1 - 10 of 366 |
Quality Assurance Unit Associate III (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 ... - Sep 15
Clinical Trial Manager
Bayside Solutions
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Santa Clara, CA, 95053
... experienced Clinical Operations Professional with technical expertise in managing Phase I-III clinical trials within an industry setting and a solid understanding of clinical operations, Good Clinical Practice (GCP), and FDA regulatory requirements. ... - Sep 15
Staff Microbiology Scientist
Sterling Engineering
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San Jose, CA, 95134
$65-70 / hour
... Ensure compliance with regulatory standards (e.g., FDA, ISO) and comply with biohazard safety standards. Participate in product risk assessment, technical design reviews and critically evaluate design and implementation plans. Summarize findings and ... - Sep 13
Technical Writer
Balance Staffing Company
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San Jose, CA
... · Experience working in a regulated industry such as FDA or ISO. · Experience with electronic document management software (Livelink or similar) for tracking and processing document change requests. · Experience with Quality Management System. · ... - Sep 20
Med Device Assembler II
inSync Staffing
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San Jose, CA, 95131
... Follow general safety rules, manufacturing procedures, company policies, and FDA regulations. Complete device history records using good documentation practices. Perform additional tasks as required. Education Requirements: High school diploma or ... - Sep 22
Clinical Trial Manager / Senior Clinical Trial Manager
Bayside Solutions
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Santa Clara, CA, 95053
... with technical expertise in managing Phase I-III clinical trials in an industry setting and who has a strong knowledge of clinical operations, Good Clinical Practice (GCP), and US Food and Drug Administration (FDA) regulatory requirements. ... - Sep 15
Med Device Assembler III
inSync Staffing
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San Jose, CA, 95131
... Follow general safety rules, manufacturing procedures, company policies, and FDA regulations. Monitor in-process controls and test yields to ensure manufacturing processes operate within approved specifications. Complete device history records using ... - Sep 22
Quality Manager
ATR International
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Milpitas, CA
90000USD - 125000USD per year
... · Directly responsible for the creation and maintenance of the Quality Management System that is in full compliance to the existing (and when needed, future) ISO and regulatory standards such as ISO 9001, ISO 13485, ISO 14001, and/or FDA etc. · Lead ... - Sep 10
Senior Research And Development Engineer
Galaxy Therapeutics
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Milpitas, CA, 95035
... Having successfully demonstrated proof of concept, clinical safety, and efficacy with our Pre SEAL IT trial, we are now working with the FDA to launch our Pre-Market Approval SEAL-IT trial in the US and internationally. Our core team, based in ... - Sep 19
Sr. Supplier Quality Engineer
Shockwave Medical
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Santa Clara, CA, 95053
... Orders (DCOs) Provide technical support and guidance to the Quality Assurance group Support internal and third-party audits (FDA, Notified Body) Participate in Material Review Board (MRB) meetings Manufacturing Line Transfers Partner with cross ... - Aug 27