| Resume alert | Resumes 81 - 90 of 828 |
Customer Service Production Supervisor
Hayward, CA
... and medical devices production environments including RMA Repair, Manufacturing, Customer Service, Quality Assurance and Logistic Warehousing SUMMARY OF QUALIFICATIONS Familiar with FDA Quality System, ISO 13485, 9001 and IPC-A-610 Standards. ... - 2023 Jan 25
... and medical devices production environments including RMA Repair, Manufacturing, Customer Service, Quality Assurance and Logistic Warehousing SUMMARY OF QUALIFICATIONS Familiar with FDA Quality System, ISO 13485, 9001 and IPC-A-610 Standards. ... - 2023 Jan 25
Senior TMS supervising Psychiatric physician
Los Altos Hills, CA
... 2-Silicon Valley Transcranial Magnetic Stimulation (TMS): founder and medical director providing state of the arts, FDA approved treatment that is noninvasive, without systemic side effects for the treatment of depression. Jan 2011-Present. We have ... - 2023 Jan 11
... 2-Silicon Valley Transcranial Magnetic Stimulation (TMS): founder and medical director providing state of the arts, FDA approved treatment that is noninvasive, without systemic side effects for the treatment of depression. Jan 2011-Present. We have ... - 2023 Jan 11
Active Directory Engineer
Fremont, CA, 94555
... Experienced in Regulatory environment, FDA compliance. Design of process improvement for ongoing support, operationalization of implemented solutions, and transition of ongoing tasks to support staff. Good knowledge of ITIL (IT service management). ... - 2023 Jan 10
... Experienced in Regulatory environment, FDA compliance. Design of process improvement for ongoing support, operationalization of implemented solutions, and transition of ongoing tasks to support staff. Good knowledge of ITIL (IT service management). ... - 2023 Jan 10
Research Scientist Investigator
South San Francisco, CA
... The training consisted of interactive training with NIH directors and industry executives which included details in clinical trials, developmental stages of biologics and drugs, and FDA approval and regulations. EDUCATION Doctoral Degree (Ph.D.) in ... - 2023 Jan 08
... The training consisted of interactive training with NIH directors and industry executives which included details in clinical trials, developmental stages of biologics and drugs, and FDA approval and regulations. EDUCATION Doctoral Degree (Ph.D.) in ... - 2023 Jan 08
Contract Administrator/ Specialist
Hayward, CA
... with supporting documentation such as Independent Cost Estimate Purchase (ICE), Scope of Work, Quote Tabulation, Sole Source Justification, Cost Analysis (short form for Sole Source Contracts), FTA Require- ments if FDA, Contract Notification. ... - 2022 Dec 17
... with supporting documentation such as Independent Cost Estimate Purchase (ICE), Scope of Work, Quote Tabulation, Sole Source Justification, Cost Analysis (short form for Sole Source Contracts), FTA Require- ments if FDA, Contract Notification. ... - 2022 Dec 17
Medical Device Regulatory Affairs
San Francisco, CA
... p) I had helped clients to remediate FDA 483 and warning letters. q) Had performed many quality audits both internal and external. r) Had interacted with FDA officers many times. s) I can speak and write three languages English, Chinese (Speak, read ... - 2022 Dec 16
... p) I had helped clients to remediate FDA 483 and warning letters. q) Had performed many quality audits both internal and external. r) Had interacted with FDA officers many times. s) I can speak and write three languages English, Chinese (Speak, read ... - 2022 Dec 16
Qa Engineer Automation
Fremont, CA
... • Staff Software Engineer / Consultant @Element Science, Inc Sep 18 – Dec 18 * Executed the software engineering verification for a FDA regulated class C Data Analysis Application Software (as a class3 life-saving medical device). * Improved & ... - 2022 Nov 29
... • Staff Software Engineer / Consultant @Element Science, Inc Sep 18 – Dec 18 * Executed the software engineering verification for a FDA regulated class C Data Analysis Application Software (as a class3 life-saving medical device). * Improved & ... - 2022 Nov 29
Quality Engineer Document Control
Milpitas, CA, 95035
... SURGICAL – Santa Clara, CA Vice President of Quality Assurance Responsible for developing, implementing, and maintaining a quality management system compliant with FDA QS Regulation, EN/ISO 13485, MDD, and Canadian Medical Devices Regulations. ... - 2022 Nov 08
... SURGICAL – Santa Clara, CA Vice President of Quality Assurance Responsible for developing, implementing, and maintaining a quality management system compliant with FDA QS Regulation, EN/ISO 13485, MDD, and Canadian Medical Devices Regulations. ... - 2022 Nov 08
Pharmacovigilance Scientist
Fremont, CA
... clients’ procedures and international drug safety regulations including- ICH guidelines on safety and efficacy, Volume 9A, FDA guidelines, CIOMS, new EU PV legislation Drug Safety Associate, Johnson & Johnson Pharmaceuticals, New Brunswick, NJ Sep ... - 2022 Oct 19
... clients’ procedures and international drug safety regulations including- ICH guidelines on safety and efficacy, Volume 9A, FDA guidelines, CIOMS, new EU PV legislation Drug Safety Associate, Johnson & Johnson Pharmaceuticals, New Brunswick, NJ Sep ... - 2022 Oct 19
Safety Officer Program Manager
San Ramon, CA
... that touches the baby’s eye to locate indicators to catch diseases early · Secured FDA and ISO approvals and sold devices worldwide · First to introduce product software validation concepts to Mattson, building the system and teaching the benefits. ... - 2022 Oct 04
... that touches the baby’s eye to locate indicators to catch diseases early · Secured FDA and ISO approvals and sold devices worldwide · First to introduce product software validation concepts to Mattson, building the system and teaching the benefits. ... - 2022 Oct 04