| Distance: |
Resume alert |
Resumes 191 - 200 of 25458 |
Philadelphia, PA
... EXPERIENCE November 2025 - Current CSL Plasma • Performed venipuncture and plasma collection procedures following FDA, OSHA, and company regulationConfidently and carefully drew blood from patients of all ages.Performed venipuncture and plasma ...
- Jan 12
Leesburg, FL, 34748
... • CGMP • Order Picking • English • Proactiveness • Laboratory experience • Stocking • Assembly • Attention to detail • FDA regulations • Computer skills • Quality Inspection • Interpersonal skills • Cash handling • Warehouse Experience • Line ...
- Jan 12
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
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
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
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
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
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
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
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