| Resume alert | Resumes 21 - 30 of 748 |
Software Engineer C++
Santa Clara, CA, 95050
... • FDA Validation experience with Semiconductor, medical devices and pharmaceutical manufacturing. • Experienced with gas sampling inlets and measuring systems. • Embedded Systems Programming – 80x86 assembler, Forth, C, C++ and C#. • Programming ... - Feb 07
... • FDA Validation experience with Semiconductor, medical devices and pharmaceutical manufacturing. • Experienced with gas sampling inlets and measuring systems. • Embedded Systems Programming – 80x86 assembler, Forth, C, C++ and C#. • Programming ... - Feb 07
Inventory Control Supply Chain
Fremont, CA
... Expertise in FDA Rules: Manage GMP inventory throughout the SCM, ensure drug accountability Experience of a practical application of U.S and international medical device regulations (IDMRF), FDA, 21 CFR Part 820, ISO 13485, European Device ... - Jan 25
... Expertise in FDA Rules: Manage GMP inventory throughout the SCM, ensure drug accountability Experience of a practical application of U.S and international medical device regulations (IDMRF), FDA, 21 CFR Part 820, ISO 13485, European Device ... - Jan 25
Quality Assurance Document Control
Oakland, CA
... *QI: Verify material's are labled according to build of materials and component formulation (FDA Approved). * Collect and delivery all product at the component level * Complete Documentaion of product that is placed into inventory for back-fill for ... - Jan 25
... *QI: Verify material's are labled according to build of materials and component formulation (FDA Approved). * Collect and delivery all product at the component level * Complete Documentaion of product that is placed into inventory for back-fill for ... - Jan 25
Supply Chain Vice President
Fremont, CA, 94536
... Adept in major FDA, DEA, EFSA and internal audits. An adroit leader, able to adequately manage the staff of 180+ people. Possess strong decision-making and problem-solving skills needed to identify cost-saving opportunities, lead time compliance, ... - Jan 22
... Adept in major FDA, DEA, EFSA and internal audits. An adroit leader, able to adequately manage the staff of 180+ people. Possess strong decision-making and problem-solving skills needed to identify cost-saving opportunities, lead time compliance, ... - Jan 22
Engineering Technician III
Hayward, CA
Arnold Blanco ad2wjc@r.postjobfree.com • 510-***-**** Senior Technician Technician with 20+ years’ experience in a manufacturing environment with 4 years in Quality Assurance and an extensive background in cGMP, FDA, ISO, Clean Room, and ITAR ... - Jan 18
Arnold Blanco ad2wjc@r.postjobfree.com • 510-***-**** Senior Technician Technician with 20+ years’ experience in a manufacturing environment with 4 years in Quality Assurance and an extensive background in cGMP, FDA, ISO, Clean Room, and ITAR ... - Jan 18
Information Technology Medical Devices
Menlo Park, CA, 94025
... 60950, as well as FDA regulations (21CFR820), ISO 13485, and the 510(K) clearance process. Skilled in managing projects, with excellent communication and interpersonal abilities. Highly self-motivated and dedicated to ensuring the safety and ... - Jan 18
... 60950, as well as FDA regulations (21CFR820), ISO 13485, and the 510(K) clearance process. Skilled in managing projects, with excellent communication and interpersonal abilities. Highly self-motivated and dedicated to ensuring the safety and ... - Jan 18
Data Analyst Analysis
Cupertino, CA
... Designed and automated the MAUDE process for RPMS team which performs monthly review of device related complaints from FDA and tracks it in SQL database. Created a master data for all complaints related to Intuitive’s products and managed this data ... - Jan 18
... Designed and automated the MAUDE process for RPMS team which performs monthly review of device related complaints from FDA and tracks it in SQL database. Created a master data for all complaints related to Intuitive’s products and managed this data ... - Jan 18
Software Engineer C++
Milpitas, CA
... ● Evaluated Hematology products as per FDA standards. TECHNICAL SKILLS Hardware Renesas Controllers: R8C, H8S; Nordic: nRF52x; Cypress PSoC; PowerPC: MPC850, MPC852T, MPC8323E, MPC8360, MPC5553; OMAP Controller ARM: LPC17xx; 8255, 8259 Device Driver ... - Jan 09
... ● Evaluated Hematology products as per FDA standards. TECHNICAL SKILLS Hardware Renesas Controllers: R8C, H8S; Nordic: nRF52x; Cypress PSoC; PowerPC: MPC850, MPC852T, MPC8323E, MPC8360, MPC5553; OMAP Controller ARM: LPC17xx; 8255, 8259 Device Driver ... - Jan 09
Data Entry Patient Care
San Francisco, CA, 94102
... ●Understanding of Drug Safety Surveillance and the FDA Adverse Event Reporting System (FAERS). ●Experienced in adverse event reporting using the voluntary MedWatch 3500 (for HCP and consumer) and MedWatch 3500 B (consumer-friendly version of 3500) ... - 2023 Dec 30
... ●Understanding of Drug Safety Surveillance and the FDA Adverse Event Reporting System (FAERS). ●Experienced in adverse event reporting using the voluntary MedWatch 3500 (for HCP and consumer) and MedWatch 3500 B (consumer-friendly version of 3500) ... - 2023 Dec 30
A Contractor Senior
Redwood City, CA
... ●Performed Peptide Mapping, Carbohydrate testing with the FDA-approved products. ●Reviewed the testing records in the QC lab for the release of products including small and large molecules. ●Expert in QC investigation for OOS testing. Expert in QC ... - 2023 Dec 27
... ●Performed Peptide Mapping, Carbohydrate testing with the FDA-approved products. ●Reviewed the testing records in the QC lab for the release of products including small and large molecules. ●Expert in QC investigation for OOS testing. Expert in QC ... - 2023 Dec 27