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FDA resumes in Jersey City, NJ

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Resume alert Resumes 61 - 70 of 1416

Quality Assurance Regulatory Affairs

Irvington, NJ
... s production activities comply with government regulation SUMMARY OF TECHNICAL SKILLS High level of understanding of applicable regulations, including FDA (21CFR 312 and 314), ICH (E2A, E2B, E2C), GCP guidelines, EMA regulations, GVP Modules, etc. ... - Jan 15

Pharmacy Technician Customer Service

Carteret, NJ
... Skills: • MS Office • Pharmacy Calculations • Compounding medication following aseptic techniques • Injections • Sterile Preparations • Prescription Process • Drug Classification & Safety • Medicine Inventory • FDA Compliance • Customer Service ... - Jan 14

Experienced Hands-On Chief Technology Officer

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

Clinical Research Senior

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

Customer Service Pharmacy Technician

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

Quality Control Machine Operator

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

Clinical Research Data Management

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

Assistant Director Clinical Pharmacist

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

Project Manager Clinical Trial

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

Human Resources Manager

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
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