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Resumes 341 - 350 of 25456 |
Ocklawaha, FL
... Followed OSHA, FDA and AAMI guidelines related to sterilization in compliance with administrative regulations. Collaborated with medical staff to confirm availability of medical equipment for patient care. Troubleshot medical equipment malfunctions ...
- 2025 Nov 28
Springfield, MA
... identifying red blood cell morphologies, platelet abnormalities, and blood parasites in 12+ species • Running samples from FDA-approved research experiments to assist with discovering proper treatment for animals PACKAGE DELIVERY DRIVER Vista, CA ...
- 2025 Nov 28
North Scituate, RI
... • Lead of various laboratory projects for constant improvements to laboratory practices, workloads, and turnaround times • Laboratory lead for Client and FDA Audits September 2013 – September 2015 Finished Product Supervisor, Denison Pharmaceuticals ...
- 2025 Nov 27
San Carlos Park, FL, 33908
... • Oversaw global import/export documentation and regulatory compliance (IATA, FDA, HIPAA, DOT). • Monitored global inventories, retest dating, and proactively identified risks with corrective action plans. • Partnered cross-functionally with CMC, ...
- 2025 Nov 26
Hopkinton, MA
... Completed comprehensive training through Clinical Research Fastrack, gaining knowledge in FDA regulations, trial operations, informed consent, and site management. Passionate about contributing to high-quality, patient-centered studies that advance ...
- 2025 Nov 26
West Roxbury, MA
... Skilled in FDA 510(k), ISO 13485, EU MDR, and PMS processes. Founder of an AI-powered compliance platform and Co-founder of Path2RAQA, which streamlines the regulatory affairs journey & got featured in Times Square for regulatory innovation. ...
- 2025 Nov 24
Illinois
... and Assessment, ASQC Communicative Manager Course En 46001, GMP, and FDA training course Continuous Improvement of process course Problem Solving training workshop course Design of experiment APQP, PPAP, FMEA, DOE, and PFMEA courses and training. ...
- 2025 Nov 24
Philadelphia, PA
... Safety Narratives Investigators Brochures Periodic Update Safety Reports Marketing Authorization Applications Responses to FDA Questions Medical Device CERs Updates to SOPs Education MA Clinical Psychology, University of Pennsylvania, Philadelphia, ...
- 2025 Nov 24
Anaheim, CA
... Experienced in FDA 510k submissions, EU-MDR Gap Mitigation’s. GMP, TUV, MATLAB, SPC, SIX SIGMA and ISO 9000, ISO 14971, ISO 13824, and ISO 13408. Product verification IQ, OQ, PQ. Hydro coater 4up and 8up automation design, and assembly utilizing ...
- 2025 Nov 24
Philadelphia, PA
... high priority change controls needed for production Provided reports and documents per audit requests, both internal and FDA Process, distribute and file Raw Material and Finished Product Test Methods & Analytical Reports Issue and track process ...
- 2025 Nov 24