| Resume alert | Resumes 1 - 10 of 320 |
Assay Development Data Analysis
San Diego, CA, 92101
... • Spearheaded development and validation of multiple FDA approved/510k CLIA-Waived medical devices for infectious diseases, such as Covid, influenza A/B, RSA, Strep A, Mono. Developed and validated Quantitative Vitamin D assay. • Conceptualized and ... - Jun 21
... • Spearheaded development and validation of multiple FDA approved/510k CLIA-Waived medical devices for infectious diseases, such as Covid, influenza A/B, RSA, Strep A, Mono. Developed and validated Quantitative Vitamin D assay. • Conceptualized and ... - Jun 21
Medical Device Devices
Santee, CA
... Hands-on experience obtaining Regulatory Approvals for medical devices, CE, PMA, IDE and 510(k), Australia, Asia Pacific and other regions Quality assurance ISOand EN and FDA and specialty documentation needs for GMP GLP and GCP compliance. Software ... - Jun 14
... Hands-on experience obtaining Regulatory Approvals for medical devices, CE, PMA, IDE and 510(k), Australia, Asia Pacific and other regions Quality assurance ISOand EN and FDA and specialty documentation needs for GMP GLP and GCP compliance. Software ... - Jun 14
Continuous Improvement Supply Chain
Tijuana, Baja California, Mexico
... Automotive, Medical, Food, Agribusiness and Cosmetics Industry according to AS 9145 IATF 16949 ISO 13485 ISO 22 000 ISO 14971 MIL STD, FAA, FDA and Mexican NMX ARRK Product Development Group USA, INC/ ARRK Product Development Group Mexico S.A. ... - Jun 03
... Automotive, Medical, Food, Agribusiness and Cosmetics Industry according to AS 9145 IATF 16949 ISO 13485 ISO 22 000 ISO 14971 MIL STD, FAA, FDA and Mexican NMX ARRK Product Development Group USA, INC/ ARRK Product Development Group Mexico S.A. ... - Jun 03
Operations, Manufacturing & Engineering Management Professional
Chula Vista, CA
... o Implemented new and directed sustaining of regulatory compliance such as AS 9100, ISO 9001, ISO 14001, ISO 13485 & FDA requirements, ITAR Regulations, EU Standards, IPCA, and Mil-Spec Qualifications. Saied Rahimi ad5zku@r.postjobfree.com Page 3 ... - May 27
... o Implemented new and directed sustaining of regulatory compliance such as AS 9100, ISO 9001, ISO 14001, ISO 13485 & FDA requirements, ITAR Regulations, EU Standards, IPCA, and Mil-Spec Qualifications. Saied Rahimi ad5zku@r.postjobfree.com Page 3 ... - May 27
Household Manager/ Nanny
San Diego, CA
... Food and Drug Administration (FDA) approved vaccine to prevent COVID-19. Read this Fact Sheet for information about the Pfizer-BioNTech COVID-19 Vaccine. Talk to the vaccination provider if you have questions. It is your choice to receive the Pfizer ... - May 22
... Food and Drug Administration (FDA) approved vaccine to prevent COVID-19. Read this Fact Sheet for information about the Pfizer-BioNTech COVID-19 Vaccine. Talk to the vaccination provider if you have questions. It is your choice to receive the Pfizer ... - May 22
Quality Assurance Business Systems
San Diego, CA
... MAR 2017 - JUN 2019 Senior Software Test Engineer, Prometheus Laboratories, San Diego Conducted comprehensive risk assessments aligning with specific requirements Executed software validation to ensure FDA and ISO standards compliance Performed ... - May 21
... MAR 2017 - JUN 2019 Senior Software Test Engineer, Prometheus Laboratories, San Diego Conducted comprehensive risk assessments aligning with specific requirements Executed software validation to ensure FDA and ISO standards compliance Performed ... - May 21
Quality, Lab technician, Supply Chain Inventory Control
San Diego, CA
... ● Roles include Quality, Quality Document Control, Lab Roles, Analytical Chemistry, Liquid Chromatography ( HPLC ), Toxicology Synthetic testing, MRB Inventory Coordinator,, and Logistics, FDA labelling, all positions compiled in a Bioscience ... - May 15
... ● Roles include Quality, Quality Document Control, Lab Roles, Analytical Chemistry, Liquid Chromatography ( HPLC ), Toxicology Synthetic testing, MRB Inventory Coordinator,, and Logistics, FDA labelling, all positions compiled in a Bioscience ... - May 15
Technical Writer Medical Device
San Diego, CA
... Achieved 510(k) premarket notification clearance for two FDA Class II medical devices (orthodontic ceramic brackets – K130446 and K132368). As General Services Administration (GSA) proposal manager, was responsible for the award of a five-year ... - May 14
... Achieved 510(k) premarket notification clearance for two FDA Class II medical devices (orthodontic ceramic brackets – K130446 and K132368). As General Services Administration (GSA) proposal manager, was responsible for the award of a five-year ... - May 14
Document Control Auto Cad
San Diego, CA, 92101
... • Maintaining documentation in preparation for future FDA Sox audits. DJO Global, San Diego, CA Document Specialist Dec 2013 - Jul 2014 • Working in DJO's PDM department, responsible for auditing Word Documents, Solid Works, Auto Cad Drawings ... - May 14
... • Maintaining documentation in preparation for future FDA Sox audits. DJO Global, San Diego, CA Document Specialist Dec 2013 - Jul 2014 • Working in DJO's PDM department, responsible for auditing Word Documents, Solid Works, Auto Cad Drawings ... - May 14
Test Engineer Electrical
San Diego, CA
... pulse generator devices • Identified root cause and troubleshoot defective electroporation medical devices • Complied with the FDA policies, guidelines and regulatory requirements • Performed and documented all activities in compliance with Good ... - May 02
... pulse generator devices • Identified root cause and troubleshoot defective electroporation medical devices • Complied with the FDA policies, guidelines and regulatory requirements • Performed and documented all activities in compliance with Good ... - May 02