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Resumes 31 - 40 of 1038 |
Brooklyn, NY
... mobile, desktop, and web applications, both onsite and remote Build and manage team developing Software As A Medical Device (FDA regulated) Accomplishments Obtained patents related to color analysis (Business Intelligence) Opened 2 overseas (India) ...
- Jan 12
New York, NY
... • Supervised personnel in preparing timelines, SOPs, and ICF, and resolved deviations, adhering to FDA, ICH, and GCP guidelines. Clinical Data Associate DOCS Global, contracted with Abraham Cancer Center, University of Pennsylvania, Philadelphia, PA ...
- Jan 12
North Bergen, NJ
... skills Manual and automated medication dispensing Updating medication histories Prepare bubble packs Typing medication labels FDA Drug Safety Guidelines Speak Korean and English Fast learn everything and very patient listening well from others and ...
- Jan 11
Teaneck, NJ
... 2023 Clinical Research Training covering Core Competencies including: ICH GCP E6 R (2) FDA Regulations 21CFR 11, 50, 54, 56 and the Common Rule 45CFR46 Data Management Informed Consent Process Clinical Trial Operations from feasibility through close ...
- Jan 08
New York, NY
... IV Iron Therapy Protocol for Adults versus Pediatrics with alternate agents due to FDA approval of Venofer in Adults only and Ferrlicit in both. Protocol for Entereg use post GI surgery, Proper EASE REMS requirement fulfillment, and prescriber ...
- Jan 06
Teaneck, NJ, 07666
... Additional Information - Skills: Regulatory expertise: Medical Devices cGMP (21CFR Part 820 and others), ISO-13485, NSF, FDA, OSHA, EPA, AS- 9100, ISO-9000 Computer skills: SAP, WMS, BPCS-AS 400, MS Office, CMMS, ECI Fluent in Spanish US Citizen
- Jan 03
New Milford, NJ
... Involved in activities related to the project using GAMP5, ISO, FDA QSR, 21 CFR Part 11. Extensive Device specific engineering and development, and manufacturing for Classes II & III, ISO 9001, ISO Involved in packaging process development ...
- 2023 Dec 28
Uniondale, NY
... Making sure team members adhere to good manufacturing procedures "GMP", standard operating procedures "SOP", FDA and UL procedures. Dude University 3 Years Established CMMS system, utilizing Dude Solutions Software. Managed staff of 140, created ...
- 2023 Dec 27
Hicksville, NY
... Environment: Angular, Typescript, React, TensorFlow, JupyterHub, Jenkins, Docker, PostgreSQL, VSCode, GIT, Ansible, MobaXterm Leidos (Silver Spring, MD) Dec 2020-Jul 2021 Full Stack Developer Description: FDA fulfills this responsibility by ensuring ...
- 2023 Dec 23
New York, NY
... — New York, NY 03/2015 to 03/2017 Maintained clean work environment in adherence to State, FDA, and OSHA requirements Improved quality and growth of company by using Tapper and Painting skills Promoted team safety by keeping work areas free of ...
- 2023 Dec 21