| Job alert | Jobs 1 - 10 of 408 |
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
Senior Quality Engineer
Galaxy Therapeutics
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Milpitas, CA, 95035
... We are currently working with FDA to launch our Pre-Market approval SEAL-IT trial in US and internationally. Galaxy holds multiple patents in US, EU, China and other markets. Founded by four practicing neuro interventional physicians. Our core team ... - Sep 26
Assembler
CathX Medical
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Sunnyvale, CA, 94088
23USD - 28USD per hour
... 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 ... - Sep 27
Project Manager
CathX Medical
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Sunnyvale, CA, 94088
74000USD - 119000USD per year
... management of new product development and transfer to manufacturing by performing the following duties personally or through This role complies to FDA QSR (21 CFR 820), ISO 13485 requirements and adheres to the Quality Management System (QMS). ... - Sep 27
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 26
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 26
Senior Manufacturing Engineer
Elixir Medical Corporation
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Milpitas, CA, 95035
... equipment issues Work with the R&D team to develop and optimize manufacturing processes Maintain compliance with FDA and ISO guidelines for medical device development and manufacturing Maintain compliance with all document and procedure ... - Sep 26
Sr. Technical Writer
Yoh
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San Jose, CA, 95134
... writing for medical device or pharmaceutical development process (protocols, development plans, reports) Experience in: IVD or Pharmaceutical technical writing with R&D Design history files (DHF) Working in a regulated industry such as FDA or ISO. ... - Sep 26
Quality Inspector
CathX Medical
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Sunnyvale, CA, 94088
23USD - 34USD per hour
... This role complies to FDA QSR (21 CFR 820), ISO 13485 requirements and adheres to the Quality Management System (QMS). ESSENTIAL FUNCTIONS: Interprets engineering drawings per ASME Y 5 and GD&T standards, interpret standard measurement units and ... - Sep 28
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 26