| Resume alert | Resumes 71 - 80 of 585 |
Sas Programmer Data Analyst
Fremont, CA
... Created Patient narratives and generated .XML outputs for FDA regulatory submissions. Worked closely with team Statistician and prepared Adhoc reports for analysis. Created edit check programs to find data discrepancies in raw datasets. Programed ... - 2023 May 25
... Created Patient narratives and generated .XML outputs for FDA regulatory submissions. Worked closely with team Statistician and prepared Adhoc reports for analysis. Created edit check programs to find data discrepancies in raw datasets. Programed ... - 2023 May 25
Medical Writer Technical
San Jose, CA
... • Have an insight on ICH, EMA and FDA guidelines. Participated in Hackathon event, where I gained exposure in Design thinking and prototype building. • - 2023 May 02
... • Have an insight on ICH, EMA and FDA guidelines. Participated in Hackathon event, where I gained exposure in Design thinking and prototype building. • - 2023 May 02
Data Entry Project Manager
San Jose, CA
... Additionally, I am well-versed in drug safety and pharmacovigilance processes, as well as validation & verifications standards per regulatory mandates (i.e., FDA’s21 CFR Part 11, EU Annex 11, GxP, HIPAA, GDPR, including GAMP principles). As a PMI ... - 2023 Apr 21
... Additionally, I am well-versed in drug safety and pharmacovigilance processes, as well as validation & verifications standards per regulatory mandates (i.e., FDA’s21 CFR Part 11, EU Annex 11, GxP, HIPAA, GDPR, including GAMP principles). As a PMI ... - 2023 Apr 21
Data Entry Clean Room
San Jose, CA
... Adhere to general safety rules, manufacturing procedures, company policies and procedures, ISO, QSR, and FDA regulations Completion of cross-training in three or more product areas is required Perform in-process quality checks on sub-assemblies and ... - 2023 Mar 28
... Adhere to general safety rules, manufacturing procedures, company policies and procedures, ISO, QSR, and FDA regulations Completion of cross-training in three or more product areas is required Perform in-process quality checks on sub-assemblies and ... - 2023 Mar 28
Sqa Engineer Qa
Mountain View, CA, 94041
... HANCOCK MEDICAL / BEDDR SLEEP INC, MOUNTAIN VIEW, CA LEAD SQA Engineer, July 2018– August 2019 ● The Beddr Sleep Tuner is an FDA Registered medical device that has the potential to replicate the sleep lap. ● Being the first and only tester I was ... - 2023 Mar 23
... HANCOCK MEDICAL / BEDDR SLEEP INC, MOUNTAIN VIEW, CA LEAD SQA Engineer, July 2018– August 2019 ● The Beddr Sleep Tuner is an FDA Registered medical device that has the potential to replicate the sleep lap. ● Being the first and only tester I was ... - 2023 Mar 23
Mechanical Engineer Quality
San Jose, CA
... Experience in Quality Engineering, QMS, Lean Manufacturing, Process Improvement, CAPA Management, New Product Process Verification & Validation, Risk Management and Quality Assurance in compliance with FDA regulations. Provide support with BOM and ... - 2023 Mar 16
... Experience in Quality Engineering, QMS, Lean Manufacturing, Process Improvement, CAPA Management, New Product Process Verification & Validation, Risk Management and Quality Assurance in compliance with FDA regulations. Provide support with BOM and ... - 2023 Mar 16
Production / distribution supervisor
Santa Clara, CA, 94544
... •Kept areas in the warehouse sanitized and clean according to FDA laws. •Perform order-building tasks around the warehouse as needed. •Made accurate inventory counts of products and money saved at the end of the period. •Making tags and setting ... - 2023 Feb 15
... •Kept areas in the warehouse sanitized and clean according to FDA laws. •Perform order-building tasks around the warehouse as needed. •Made accurate inventory counts of products and money saved at the end of the period. •Making tags and setting ... - 2023 Feb 15
Qc Inspector Assurance
San Jose, CA
... Maintained strict FDA procedures in as fast-paced environment. Maintained accurate daily cycle counts by comparing inventory with actual product through SAP. Worked with engineering to implement design changes to enhance product reliability and ... - 2023 Feb 03
... Maintained strict FDA procedures in as fast-paced environment. Maintained accurate daily cycle counts by comparing inventory with actual product through SAP. Worked with engineering to implement design changes to enhance product reliability and ... - 2023 Feb 03
Customer Service Software Engineer
Fremont, CA
... focus while meeting stringent delivery timelines • Managed budget, schedule, resources, risks, and scope of high-value FDA-regulated products • Successfully delivered multiple product releases while consistently meeting compliance requirements ... - 2023 Jan 29
... focus while meeting stringent delivery timelines • Managed budget, schedule, resources, risks, and scope of high-value FDA-regulated products • Successfully delivered multiple product releases while consistently meeting compliance requirements ... - 2023 Jan 29
Document Control Data Entry
Hayward, CA, 94544
... GANADEN aduyik@r.postjobfree.com Brentwood, Ca 94513 925-***-**** SUMMARY: QA Documentation Specialist with experience in Documentation and Quality Assurance in FDA, GMP, GDP and GLP Environment and ISO13485. Trained on Personnel Protective ... - 2023 Jan 26
... GANADEN aduyik@r.postjobfree.com Brentwood, Ca 94513 925-***-**** SUMMARY: QA Documentation Specialist with experience in Documentation and Quality Assurance in FDA, GMP, GDP and GLP Environment and ISO13485. Trained on Personnel Protective ... - 2023 Jan 26