| Resume alert | Resumes 1 - 10 of 585 |
Manufacturing Associate Microsoft Office
San Jose, CA
... com **** ** ***** ***, *** Jose, CA 95131 408-***-**** PROFESSIONAL SUMMARY • Twenty plus years of working experience in a fast paced, small, and middle-sized pharmaceutical company with sound cGMP practice in a regulated FDA environment. ... - Sep 19
... com **** ** ***** ***, *** Jose, CA 95131 408-***-**** PROFESSIONAL SUMMARY • Twenty plus years of working experience in a fast paced, small, and middle-sized pharmaceutical company with sound cGMP practice in a regulated FDA environment. ... - Sep 19
Test Engineer Software QA
San Jose, CA
Dennis Zasoba San Jose, CA ***** ad8rzd@r.postjobfree.com Senior Quality Assurance Test Engineer A well-qualified Software Test Engineer with advanced experience in regulated environments (FDA). Skilled in managing QA teams, training in-house and ... - Sep 16
Dennis Zasoba San Jose, CA ***** ad8rzd@r.postjobfree.com Senior Quality Assurance Test Engineer A well-qualified Software Test Engineer with advanced experience in regulated environments (FDA). Skilled in managing QA teams, training in-house and ... - Sep 16
Ux Designer Ui
San Jose, CA
... • Demonstrated experience in the medical product industry with a strong understanding of IEC 62366-1 and FDA Human Factors Guidance. Proficient in IEC 62304 (software lifecycle processes for medical devices), ensuring compliance and usability in ... - Sep 13
... • Demonstrated experience in the medical product industry with a strong understanding of IEC 62366-1 and FDA Human Factors Guidance. Proficient in IEC 62304 (software lifecycle processes for medical devices), ensuring compliance and usability in ... - Sep 13
Supply Chain Project Manager
San Jose, CA
... • Knowledge of GMP, FDA guidelines, working knowledge of Medical Device regulations including ISO13485 and 21 CFR 820. • Responsible for UL, ISO and FDA Audits audits to ensure compliance to regulatory and statutory requirements, EH&S (Environmental ... - Sep 08
... • Knowledge of GMP, FDA guidelines, working knowledge of Medical Device regulations including ISO13485 and 21 CFR 820. • Responsible for UL, ISO and FDA Audits audits to ensure compliance to regulatory and statutory requirements, EH&S (Environmental ... - Sep 08
Medical Device Regulatory Compliance
Santa Clara, CA
... • Proficient in clinical & regulatory compliance (FDA, ISO, ANSI), technology migration, and mergers/acquisitions pulling into operations to produce high quality products from recently acquired technologies in a timely manner. • Exploiting ... - Sep 05
... • Proficient in clinical & regulatory compliance (FDA, ISO, ANSI), technology migration, and mergers/acquisitions pulling into operations to produce high quality products from recently acquired technologies in a timely manner. • Exploiting ... - Sep 05
Medical Device Business Development
Morgan Hill, CA
... Managed FDA registration for full regulatory compliance. Directed product selection and importation. Hired, trained and motivated team members across all aspects of the company. GS MEDICAL USA, LLC, Santa Cruz, CA (Spinal Implants Manufacturer) ... - Sep 03
... Managed FDA registration for full regulatory compliance. Directed product selection and importation. Hired, trained and motivated team members across all aspects of the company. GS MEDICAL USA, LLC, Santa Cruz, CA (Spinal Implants Manufacturer) ... - Sep 03
Customer Service Pharmacy Technician
San Jose, CA
... SKILLS • Prescription Order Verification • Confidentiality Practices • Workflow Optimization • Order Verification Heartsaver First Aid CPR AED (First Aid CPR AED) • • Data Entry • Employee Training • Customer service • FDA Drug Safety Guidelines • ... - Sep 01
... SKILLS • Prescription Order Verification • Confidentiality Practices • Workflow Optimization • Order Verification Heartsaver First Aid CPR AED (First Aid CPR AED) • • Data Entry • Employee Training • Customer service • FDA Drug Safety Guidelines • ... - Sep 01
QA, Validation, RA, Master Data Governance and Stewardship, SAP
Newark, CA, 94560
... Interface with inspectors during FDA (Food and Drug AdministraƟon), Corporate and Internal Audits. Complete responses and closure of commitments for Audits. Publish Annual Product Review (APR). Involved in Quality Systems through Change Control, ... - Aug 29
... Interface with inspectors during FDA (Food and Drug AdministraƟon), Corporate and Internal Audits. Complete responses and closure of commitments for Audits. Publish Annual Product Review (APR). Involved in Quality Systems through Change Control, ... - Aug 29
Information Management Clinical Documentation
Downtown North, CA, 94301
... 15 year of experience in Life Science working in laboratory (LMIS) with DNA extraction, develop micro assays and genome testing, and 15 plus year of FDA regulatory experience, and proficient in healthcare information management and Laboratory ... - Aug 28
... 15 year of experience in Life Science working in laboratory (LMIS) with DNA extraction, develop micro assays and genome testing, and 15 plus year of FDA regulatory experience, and proficient in healthcare information management and Laboratory ... - Aug 28
Platform Engineering
Cupertino, CA
... Over 15 years of experience with regulated environments such as HIPAA, CLIA, FDA, PCI, SOC II, GDPR, and CCPA. Papers published by IEEE and other organizations. MBA, MSEE, BSEE, and PMP (Project Management Professional.) Education: MBA, Finance, ... - Aug 26
... Over 15 years of experience with regulated environments such as HIPAA, CLIA, FDA, PCI, SOC II, GDPR, and CCPA. Papers published by IEEE and other organizations. MBA, MSEE, BSEE, and PMP (Project Management Professional.) Education: MBA, Finance, ... - Aug 26