| Resume alert | Resumes 1 - 10 of 576 |
Test Engineer Medical Device
San Jose, CA, 95126
... San Jose, CA TEST ENGINEER 8/20/2021 – 11/20/2021 Tested the wireless communication, a class 1 medical device, subject to FDA oversight · Executed Wireless Protocols Allergan, Pleasanton, CA (Contract) TEST ENGINEER 4/15/2019 – 6/20/2019 Tested ... - May 10
... San Jose, CA TEST ENGINEER 8/20/2021 – 11/20/2021 Tested the wireless communication, a class 1 medical device, subject to FDA oversight · Executed Wireless Protocols Allergan, Pleasanton, CA (Contract) TEST ENGINEER 4/15/2019 – 6/20/2019 Tested ... - May 10
Product Quality A Team
San Jose, CA
... and Improvement ● Supply Chain Management ● Quality Control ● Interviewing and Prescreening ● GMP ● CSF/Quarterly goals ● FDA Audit ● ERT Member/CRP Certified ● PCB Assembly/Soldering/Mil Spec, ● Voyager ● Jira ● AI ● Managed logistics for offsite ... - May 08
... and Improvement ● Supply Chain Management ● Quality Control ● Interviewing and Prescreening ● GMP ● CSF/Quarterly goals ● FDA Audit ● ERT Member/CRP Certified ● PCB Assembly/Soldering/Mil Spec, ● Voyager ● Jira ● AI ● Managed logistics for offsite ... - May 08
Service Representative Patient
San Jose, CA
... Ensured complaints were filed according to FDA guidelines. Assisted other staff members as needed. 03/1990 - 10/1995 Receptionist/Secretary Sumitomo Metal Industries, Santa Clara, CA Supported the Human Resources Department by answering phones, ... - May 04
... Ensured complaints were filed according to FDA guidelines. Assisted other staff members as needed. 03/1990 - 10/1995 Receptionist/Secretary Sumitomo Metal Industries, Santa Clara, CA Supported the Human Resources Department by answering phones, ... - May 04
Customer Service Quality Inspector
San Jose, CA
... Hands-on experience Agile, GMP (Good Manufacturing Practices), ERP (Enterprise Resource Planning) and SAP (Systems Application & Products) Knowledgeable of the FDA, QSR (Quality System Regulations), ISO 13485 (Quality Management System) and 14001 ... - Apr 25
... Hands-on experience Agile, GMP (Good Manufacturing Practices), ERP (Enterprise Resource Planning) and SAP (Systems Application & Products) Knowledgeable of the FDA, QSR (Quality System Regulations), ISO 13485 (Quality Management System) and 14001 ... - Apr 25
Service Technician Quality Assurance
San Jose, CA
... All work experience in ISO 13485: xx and FDA 21CFR820 environments. Involved in ISO 13485: xx and FDA 21CFR820 audits as SME. Experienced with ARENA PLM for Document Review, and NMR creation. Experience in assisting Engineering in completing IQ/OQ ... - Apr 22
... All work experience in ISO 13485: xx and FDA 21CFR820 environments. Involved in ISO 13485: xx and FDA 21CFR820 audits as SME. Experienced with ARENA PLM for Document Review, and NMR creation. Experience in assisting Engineering in completing IQ/OQ ... - Apr 22
Document Control Specialist
Milpitas, CA
... Sunnyvale CA Document Controller/ CAPA Coordinator – Issue, process and implement NOC (Notice of Change) for FDA regulated Medical Products. Assist originators with assessing levels of changes, the corresponding attachments that apply, and creating ... - Apr 16
... Sunnyvale CA Document Controller/ CAPA Coordinator – Issue, process and implement NOC (Notice of Change) for FDA regulated Medical Products. Assist originators with assessing levels of changes, the corresponding attachments that apply, and creating ... - Apr 16
Document Control Specialist
Santa Clara, CA
... the Regulatory team with preparation and assembling 510(K) and FDA Response Letters ●Received SAP training to submit POs for upcoming Notifying Bodies (NB) audits and procure the goods and services for the Quality Department Loral Space System, Mt. ... - Mar 30
... the Regulatory team with preparation and assembling 510(K) and FDA Response Letters ●Received SAP training to submit POs for upcoming Notifying Bodies (NB) audits and procure the goods and services for the Quality Department Loral Space System, Mt. ... - Mar 30
Medical Devices Inventory Control
Pleasanton, CA, 94566
... ***-**** ad4jpj@r.postjobfree.com Experienced hands-on professional with specialties in high tech,bio-technology and bio-medical devices, knowledgeable in various logistics, export and manufacturing processes of medical devices, FDA,GMP,SOP's & ISO. ... - Mar 24
... ***-**** ad4jpj@r.postjobfree.com Experienced hands-on professional with specialties in high tech,bio-technology and bio-medical devices, knowledgeable in various logistics, export and manufacturing processes of medical devices, FDA,GMP,SOP's & ISO. ... - Mar 24
Palo Alto Firmware Engineer
Menlo Park, CA
... Designed test benches for functional simulation and completed documents used for FDA clearance submission Hardware Developer September 2015 – February 2016 Xilinx IP configuration & top-level integration 1 • AXI-DMA&-GPIO data transfer • Async. ... - Mar 22
... Designed test benches for functional simulation and completed documents used for FDA clearance submission Hardware Developer September 2015 – February 2016 Xilinx IP configuration & top-level integration 1 • AXI-DMA&-GPIO data transfer • Async. ... - Mar 22
Medical Device Lean Manufacturing
San Jose, CA
... •Support for resolution of FDA audit comment concerning supporting documentation for transporting of materials. •Write and execute shipping test plan for CDMO product. Baxter Healthcare & Lonza – Hayward, CA 05/08-07/19 Validation Engineering II ... - Mar 19
... •Support for resolution of FDA audit comment concerning supporting documentation for transporting of materials. •Write and execute shipping test plan for CDMO product. Baxter Healthcare & Lonza – Hayward, CA 05/08-07/19 Validation Engineering II ... - Mar 19