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Resumes 61 - 70 of 1475 |
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
Elizabeth, NJ
... • Manufacturing (9 years) • Food Production (10+ years) • OSHA,PPE, FDA,SOP, Table Press (5 years) • Lean Manufacturing • Assembly • Leadership • Quality control • Continuous improvement • Team management • Single Punch Table Press, Pill Press. ...
- Jan 09
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
Elizabeth, NJ
... approach Strong Knowledge of GCPs, FDA, and ICH requirements Superior work ethics Excellent interpersonal and leadership skills with an eye for detail Excellent knowledge of MS Word, Access, Excel, Teams, Skype, One Note, Zoom, and Share drives. ...
- Jan 05
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
Keyport, NJ
... Central Storage Picked orders and served as a Receiving Clerk EDUCATION High School Graduate RELATED TRAINING FDA Good Manufacturing Practice Powered Industrial Lift Truck Training OSHA related training CERTIFICATIONS Certified Forklift Operator ...
- Jan 03
Piscataway, NJ
... all processes and documents for digital FDA review remotely. •Developed company expansion capacity models and execute resourcing strategies to ensure delivery of activities and scopes of work from various internal teams and external consultants ...
- Jan 02