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Distance: Resume alert Resumes 21 - 30 of 25450

Medical Device Consultant/Administrative

Clearwater, FL
... Initiate Medical Device Reports (MDR) for FDA submissions; Complete MDR/vigilance reports per client process and regulations; Regularly report to various levels of ECI/client management on the progress of Complaints and MDR; Facilitate Team Meetings ... - Jan 12

Physician Advisor - Family Medicine, Geriatrics, Obesity Medicine

Lake Mary, FL
... & Physician Training Hormone & Longevity Medicine Mission-Based Global Health Delivery Clinical Protocol Development (IRB, FDA compliance) Bilingual: English & Spanish (Colombian) LEADERSHIP ROLES & APPOINTMENTS CEO, EternaMD Medical Rejuvenation ... - Jan 12

Cyber Security Engineer - Application & Product Security Specialist

Tustin, CA
... Validated remediation and security controls for medical device software to support HIPAA and FDA compliance. Cognizant Technology Solutions Jul 2022 – Jun 2023 Product Security Developer Involved in designing and developing a secure AI-driven ... - Jan 12

Senior Oracle & Cloud Database Architect

Rio de Janeiro, Brazil
... Snowflake in critical and regulated environments (PCI, SOX, FDA), gaining an expertise in high availability (Oracle RAC, Data Guard, AlwaysOn), advanced performance tuning, and in automation with Terraform, Ansible, Shell Script, Python, and CI/CD. ... - Jan 12

Pharmacovigilance and Drug Safety Expert

Philadelphia, PA
... Perform User Acceptance TesƟng (UAT) on a new medical module designed to capture most data elements of the FDA MedWatch form. AE Data Remediator Jun 2004 to Dec 2005 Research PharmaceuƟcal Services Plymouth MeeƟng PA 19462 ResponsibiliƟes Create ... - Jan 11

Senior .NET Architect and Cloud Solutions Lead

Irvine, CA, 92606
... Atharvana Infotech, Hyderabad, TS, India as Software Engineer Oct’12 – Aug’15 Description: Vigilistics is a platform that combines automated data collection from PLCs with advanced mobility features to deliver FDA-validated compliance reporting, ... - Jan 11

Process Safety & Manufacturing Engineer Leader

Fort Wayne, IN
... ISO 9001 - 13485 Quality Management, and FDA (21 CFR 820). EXPERIENCE DOT AMERICA - Columbia City, IN ( 02/24 - 05/25 ) Process Engineer - Contractor • Responsible for Validation and Qualification of Process Equipment using IQ, OQ, and PQ in the ... - Jan 11

Emerging Healthcare Economist and Neuroimaging Researcher

Bronx, NY
... sites to ensure study access, FDA regulatory alignment, and operational feasibility. ● Managed trial wide digital modernization efforts, leading multi stakeholder workflows (Regulatory, Legal, Data Management, Clinical Science) to increase ... - Jan 11

Administrative Assistant

White Castle, LA
... reached and exceeded goals Sample and record sugar cane cores using laboratory equipment and data entry software to ensure FDA and company standards met Conduct routine ground traffic control under direct foreman supervision ensuring proper lane ... - Jan 10

Quality Assurance Engineer and Auditor

Langley, BC, Canada
... FDA, Health Canada, ISO 9001, IATF, CSA, CWB, AS9100, and ASME standards. Developed and implemented QMS frameworks, driving continuous improvement initiatives and leading cross-functional teams across global operations. Skilled in quality tools, ... - Jan 10
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