| Resume alert | Resumes 61 - 70 of 827 |
Clinical Research Project Manager
San Francisco, CA
... Proven track record of success in bringing eight drugs to FDA approval for top biotech companies. SKILLS • Project Management • Strategic Tine-line Development • Global Drug Development • Startup Design Specialist • Cross-functional Team Leadership ... - 2023 Sep 30
... Proven track record of success in bringing eight drugs to FDA approval for top biotech companies. SKILLS • Project Management • Strategic Tine-line Development • Global Drug Development • Startup Design Specialist • Cross-functional Team Leadership ... - 2023 Sep 30
Clinical Trial Research
San Francisco, CA
... and training Demonstrates expertise to support SOP development and implementation Demonstrates through knowledge of FDA and EMA Regulations, ICH Guidelines, and GCP governing the conduct of clinical studies Drafts and coordinates review of ... - 2023 Sep 27
... and training Demonstrates expertise to support SOP development and implementation Demonstrates through knowledge of FDA and EMA Regulations, ICH Guidelines, and GCP governing the conduct of clinical studies Drafts and coordinates review of ... - 2023 Sep 27
Senior Project Manager
Oakland, CA
... Core Competencies • Extensive Project Management experience in FDA-regulated industries • US FDA 21 CFR 820 (QSR/cGMP), EU IVDR/MDR, CMDR • ISO-3485, -10993, -14971, IEC60601 • Advanced Technical Writing • Proficient with MS Project, Smartsheet, MS ... - 2023 Sep 25
... Core Competencies • Extensive Project Management experience in FDA-regulated industries • US FDA 21 CFR 820 (QSR/cGMP), EU IVDR/MDR, CMDR • ISO-3485, -10993, -14971, IEC60601 • Advanced Technical Writing • Proficient with MS Project, Smartsheet, MS ... - 2023 Sep 25
Donor Care Quality Assurance
San Francisco, CA
... Across all the locations I've overseen, regulatory bodies such as the FDA, AABB, CSL, Cities, and Counties have consistently acknowledged our compliance and order. My exceptional leadership and communication skills have enabled me to collaborate ... - 2023 Sep 19
... Across all the locations I've overseen, regulatory bodies such as the FDA, AABB, CSL, Cities, and Counties have consistently acknowledged our compliance and order. My exceptional leadership and communication skills have enabled me to collaborate ... - 2023 Sep 19
Document Control Quality Assurance
San Mateo, CA
... GMP, GCP, GMED and FDA experience. ●4+ years of training experience (training new hires) and building curriculums for each department. ●Built, implemented and validated Electronic Document Management Systems for 3 companies. ●20+ years as Subject ... - 2023 Sep 09
... GMP, GCP, GMED and FDA experience. ●4+ years of training experience (training new hires) and building curriculums for each department. ●Built, implemented and validated Electronic Document Management Systems for 3 companies. ●20+ years as Subject ... - 2023 Sep 09
Project Manager Quality Consultant
Pinole, CA
... Responsible for inspection readiness and was the host for five successful audits from June 2009 to Aug 2010 (ISO 13485 -TUV, Internal, state FDA, ISO 13485-LNE/GMED, federal FDA). Culminated in FDA Inspection from 02-03 Aug 10 that resulted in the ... - 2023 Sep 06
... Responsible for inspection readiness and was the host for five successful audits from June 2009 to Aug 2010 (ISO 13485 -TUV, Internal, state FDA, ISO 13485-LNE/GMED, federal FDA). Culminated in FDA Inspection from 02-03 Aug 10 that resulted in the ... - 2023 Sep 06
Regulatory
San Francisco, CA
Jennifer Villaruz, MS 415-***-**** • https://www.linkedin.com/in/jennifervz • adzap9@r.postjobfree.com San Francisco, CA Regulatory Affairs Specialist AREAS OF EXPERTISE Regulatory Guidelines: FDA, EMA, Health Canada, PMDA, ASEAN Software ... - 2023 Aug 28
Jennifer Villaruz, MS 415-***-**** • https://www.linkedin.com/in/jennifervz • adzap9@r.postjobfree.com San Francisco, CA Regulatory Affairs Specialist AREAS OF EXPERTISE Regulatory Guidelines: FDA, EMA, Health Canada, PMDA, ASEAN Software ... - 2023 Aug 28
Validation Engineer
Emeryville, CA
... ATANU SEN Emeryville CA 1-305-***-**** adyzkk@r.postjobfree.com Summary Accomplished Validation Engineer with 7 years' experience catering to FDA and CLIA regulated healthcare and pharmaceutical Fortune 200 and 500 clients. Experience in cost ... - 2023 Aug 16
... ATANU SEN Emeryville CA 1-305-***-**** adyzkk@r.postjobfree.com Summary Accomplished Validation Engineer with 7 years' experience catering to FDA and CLIA regulated healthcare and pharmaceutical Fortune 200 and 500 clients. Experience in cost ... - 2023 Aug 16
Quality Assurance Data Migration
San Francisco, CA
... Proficiency in validating, auditing and preparing SOPs for Pharmaceuticals and medical devices as per FDA regulations and providing corresponding user training. Well experienced in writing technical documents such as Risk Assessment, Work ... - 2023 Jul 30
... Proficiency in validating, auditing and preparing SOPs for Pharmaceuticals and medical devices as per FDA regulations and providing corresponding user training. Well experienced in writing technical documents such as Risk Assessment, Work ... - 2023 Jul 30
Data Entry Document Control
Santa Clara, CA
... Enforce - through functional groups - document control requirements in order for Ariosa to meet internal and external needs according to CLIA/CAP, NY, ISO 13485, IVDD, and FDA (QSR) regulatory standards including all applicable local, state, ... - 2023 Jun 20
... Enforce - through functional groups - document control requirements in order for Ariosa to meet internal and external needs according to CLIA/CAP, NY, ISO 13485, IVDD, and FDA (QSR) regulatory standards including all applicable local, state, ... - 2023 Jun 20