| Distance: | Resume alert | Resumes 301 - 310 of 25469 |
Admin Training Coordinator
Escondido, CA
... WORK EXPERIENCE 07/2023 – 04/2025 Admin Training Coordinator Documentation - (Abbott Laboratories) Temecula, USA Executed data entry for over 5,000 training records with 98% accuracy, ensuring compliance with FDA regulations, SOPs, and DWIs. ... - 2025 Sep 24
... WORK EXPERIENCE 07/2023 – 04/2025 Admin Training Coordinator Documentation - (Abbott Laboratories) Temecula, USA Executed data entry for over 5,000 training records with 98% accuracy, ensuring compliance with FDA regulations, SOPs, and DWIs. ... - 2025 Sep 24
Information Technology Project Management
District Heights, MD
... Expertise in security and compliance frameworks including the NIST, CIS, ISO 27001/2, SOC 2, HIPAA, GDPR, and Global Cybersecurity Compliance audits including the SOC2 Type, ISO27001, FDA CFR21 Part 11, TISAX, for SaaS software products. Expertise ... - 2025 Sep 23
... Expertise in security and compliance frameworks including the NIST, CIS, ISO 27001/2, SOC 2, HIPAA, GDPR, and Global Cybersecurity Compliance audits including the SOC2 Type, ISO27001, FDA CFR21 Part 11, TISAX, for SaaS software products. Expertise ... - 2025 Sep 23
Asset Management Office Manager
Denver, CO
... reporting, and scheduling processes for biomedical operations • Coordinated team communications, training, and audits to meet FDA and corporate standards • Maintained documentation accuracy and quality system oversight Chiropractic Assistant ... - 2025 Sep 23
... reporting, and scheduling processes for biomedical operations • Coordinated team communications, training, and audits to meet FDA and corporate standards • Maintained documentation accuracy and quality system oversight Chiropractic Assistant ... - 2025 Sep 23
Executive Assistant Administrative Support
Quincy, MA
... ADMINISTRATIVE ASSISTANT, TECHNICAL OPERATIONS (CONTRACT) 07/2013 to 12/2014 Siemens Healthcare Diagnostics - Walpole, MA Reviewed and updated company assays for FDA compliance. Maintained SharePoint documentation and assisted technical operations ... - 2025 Sep 23
... ADMINISTRATIVE ASSISTANT, TECHNICAL OPERATIONS (CONTRACT) 07/2013 to 12/2014 Siemens Healthcare Diagnostics - Walpole, MA Reviewed and updated company assays for FDA compliance. Maintained SharePoint documentation and assisted technical operations ... - 2025 Sep 23
startup/cgmp/troubleshooting/prev maint./val engr/mfg engr
Wake Forest, NC
... Thomas Lauria EXPERIENCE DEPTH • Computer System Validation expert with 30+ years’ experience in FDA regulated environment • Project management skills demonstrated in multiple project environments, fast track/Legacy/Greenfield projects. Managing ... - 2025 Sep 23
... Thomas Lauria EXPERIENCE DEPTH • Computer System Validation expert with 30+ years’ experience in FDA regulated environment • Project management skills demonstrated in multiple project environments, fast track/Legacy/Greenfield projects. Managing ... - 2025 Sep 23
Regulatory Affairs Project Manager
Little Rock, AR
... with CMOs to synthesis drug substance, manufacture investigational drug product, perform release and stability testing on two novel vaccines, reported cGMP manufacturing and stability data to FDA Performed QA/QC for investigator-initiated studies; ... - 2025 Sep 23
... with CMOs to synthesis drug substance, manufacture investigational drug product, perform release and stability testing on two novel vaccines, reported cGMP manufacturing and stability data to FDA Performed QA/QC for investigator-initiated studies; ... - 2025 Sep 23
Project Manager
Downingtown, PA
... Class II and III medical devices are categories defined by the FDA based on their level of risk to patients and the required regulatory controls for their approval. Experience with Class I, II Devices: Regulatory Pathways: Manufacturers often find ... - 2025 Sep 23
... Class II and III medical devices are categories defined by the FDA based on their level of risk to patients and the required regulatory controls for their approval. Experience with Class I, II Devices: Regulatory Pathways: Manufacturers often find ... - 2025 Sep 23
Copy Editor Social Media
Morristown, NJ
... Certify that copy complies with AMA-11, brand guidelines, FDA rules and regulations. Fact-check content, validate references. Manage multiple projects simultaneously in a fast-paced environment. Motiva USA, Remote, NY Metro Area Copy Editor (April ... - 2025 Sep 23
... Certify that copy complies with AMA-11, brand guidelines, FDA rules and regulations. Fact-check content, validate references. Manage multiple projects simultaneously in a fast-paced environment. Motiva USA, Remote, NY Metro Area Copy Editor (April ... - 2025 Sep 23
QA Analyst
Tsentralny District, 220030, Belarus
... verified compliance with FDA 21 CFR Part 11. • Acted as liaison between clinicians and developers, translating business needs into detailed test documentation and acceptance criteria. EDUCATION Udemy- Software Testing Foundations Course - 2025 Sep 23
... verified compliance with FDA 21 CFR Part 11. • Acted as liaison between clinicians and developers, translating business needs into detailed test documentation and acceptance criteria. EDUCATION Udemy- Software Testing Foundations Course - 2025 Sep 23
Controls Engineer Engineering
Lancaster, PA
... FDA, GMP standards. International vendor equipment validation testing. Affiliations: 1986 - Present Thaddeus Stevens College of Technology Alumni Association Skills and Certifications: NFPA 70E Arc Flash Certified PC hardware/software, Networking as ... - 2025 Sep 23
... FDA, GMP standards. International vendor equipment validation testing. Affiliations: 1986 - Present Thaddeus Stevens College of Technology Alumni Association Skills and Certifications: NFPA 70E Arc Flash Certified PC hardware/software, Networking as ... - 2025 Sep 23