| Resume alert | Resumes 51 - 60 of 585 |
Qa Lead Quality Engineering
San Jose, CA
... ●Develop and maintain departmental documentation for procedures for meeting with FDA QSR, ISO guidelines, and 21 CFR Part 11 standards. ●Performed the SLC validation for the features under test and updated in ALM by executing the test cases in the ... - Jan 10
... ●Develop and maintain departmental documentation for procedures for meeting with FDA QSR, ISO guidelines, and 21 CFR Part 11 standards. ●Performed the SLC validation for the features under test and updated in ALM by executing the test cases in the ... - Jan 10
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
Manual Testing Qa Engineer
Morgan Hill, CA
... • Defined testing objectives, techniques, methods, and standards meeting Health Insurance Portability and Accountability Act (HIPAA) and US Food and Drug Administration (FDA) regulations for the leading Internet- Based Platform Incorporation for ... - Jan 08
... • Defined testing objectives, techniques, methods, and standards meeting Health Insurance Portability and Accountability Act (HIPAA) and US Food and Drug Administration (FDA) regulations for the leading Internet- Based Platform Incorporation for ... - Jan 08
Instructional Designer Design
San Jose, CA
... I also conduct needs Analysis, and Designed, Developed, Implement, and Evaluate (ADDIE) technical training programs for various operations such as Supply Chain, Manufacturing, Packaging, along with policies/procedures in order to Meet cGMP and FDA ... - Jan 07
... I also conduct needs Analysis, and Designed, Developed, Implement, and Evaluate (ADDIE) technical training programs for various operations such as Supply Chain, Manufacturing, Packaging, along with policies/procedures in order to Meet cGMP and FDA ... - Jan 07
Quality Assurance Specialist
Redwood City, CA
Rudolph Dizon Menlo Park, CA ***** 510-***-**** ad1msc@r.postjobfree.com HIGHLIGHTS OF QUALIFICATIONS Quality focused, diversified professional with 7+ years in an FDA regulated environment. Expertise in Customer Complaints, Quality Systems ... - 2023 Dec 01
Rudolph Dizon Menlo Park, CA ***** 510-***-**** ad1msc@r.postjobfree.com HIGHLIGHTS OF QUALIFICATIONS Quality focused, diversified professional with 7+ years in an FDA regulated environment. Expertise in Customer Complaints, Quality Systems ... - 2023 Dec 01
Mechanical Engineer
San Jose, CA
... PDM Admin o Partake in implementation process to ensure ISO/FDA compliance. o Control user and group permissions. o Create folder and file data cards in a usable manner for TRT purposes. o Review and update workflows. Pacific Biosciences, Menlo Park ... - 2023 Nov 30
... PDM Admin o Partake in implementation process to ensure ISO/FDA compliance. o Control user and group permissions. o Create folder and file data cards in a usable manner for TRT purposes. o Review and update workflows. Pacific Biosciences, Menlo Park ... - 2023 Nov 30
Mechanical Engineering Quality
Union City, CA
... Familiarity with OSHA, FDA, GMP standards. EDUCATION: Mechanical Engineering Technology Two years Southern Utah University Cedar City, Utah Three years Diploma in Mechanical Engineering Jawahar Lal Nehru Polytechnic Hyderabad, India WORK EXPERIENCE: ... - 2023 Nov 27
... Familiarity with OSHA, FDA, GMP standards. EDUCATION: Mechanical Engineering Technology Two years Southern Utah University Cedar City, Utah Three years Diploma in Mechanical Engineering Jawahar Lal Nehru Polytechnic Hyderabad, India WORK EXPERIENCE: ... - 2023 Nov 27
Software Test Engineer
San Jose, CA
... like marketing, QA, project manager and Regulatory teams Authoring Test protocols and Test reports as per FDA standards Provide training to all new hires on Computer System validation and involved in reviewing and approving of validation documents. ... - 2023 Nov 22
... like marketing, QA, project manager and Regulatory teams Authoring Test protocols and Test reports as per FDA standards Provide training to all new hires on Computer System validation and involved in reviewing and approving of validation documents. ... - 2023 Nov 22
Clinical Trial Palo Alto
Cupertino, CA
... experience with academic and industry teams • Familiar with FDA regulations • Medical writing for protocol of pre-clinical trials documents filing (US and Chinese FDA) PUBLICATIONS • Xiao Yu, Weihong Zhao, Xin Yang, Zhilian Wang, Min Hao*. ... - 2023 Nov 20
... experience with academic and industry teams • Familiar with FDA regulations • Medical writing for protocol of pre-clinical trials documents filing (US and Chinese FDA) PUBLICATIONS • Xiao Yu, Weihong Zhao, Xin Yang, Zhilian Wang, Min Hao*. ... - 2023 Nov 20
Medical Device Tech Transfer
Fremont, CA
... Select contract labs for formal stability program and product release, qualify them for compliance and GMP per FDA and Health Canada requirement. Conduct external GMP audit at contract lab, supplier, and contract manufacture in compliance with FDA, ... - 2023 Nov 17
... Select contract labs for formal stability program and product release, qualify them for compliance and GMP per FDA and Health Canada requirement. Conduct external GMP audit at contract lab, supplier, and contract manufacture in compliance with FDA, ... - 2023 Nov 17