| Resume alert | Resumes 11 - 20 of 1072 |
Data Entry Warehouse Associate
Newark, NJ
... Lupin Pharmaceuticals Somerset, NJ 01/2022 - 11/2022 Warehouse associate/Material Handler Current good manufacturing Practice regulation enforced by the FDA. Performed cycle counts and inventory control to accurately track product levels. Fastened ... - Mar 28
... Lupin Pharmaceuticals Somerset, NJ 01/2022 - 11/2022 Warehouse associate/Material Handler Current good manufacturing Practice regulation enforced by the FDA. Performed cycle counts and inventory control to accurately track product levels. Fastened ... - Mar 28
Forklift Operator Inventory Control
Newark, NJ
... • Knowledge of cGMP/FDA regulated industry Education High school diploma Piscataway High School - Piscataway, NJ Baskerville Institute Skills • Forklift • Ups/fedex • Operator certification • Time Management • Manufacturing • Warehouse management ... - Mar 26
... • Knowledge of cGMP/FDA regulated industry Education High school diploma Piscataway High School - Piscataway, NJ Baskerville Institute Skills • Forklift • Ups/fedex • Operator certification • Time Management • Manufacturing • Warehouse management ... - Mar 26
Expert Level Us Citizen
Jersey City, NJ
... June 2015 to July 2017 Pharma DSCSA Project Pharma DSCSA project is the application provided for pharmaceutical companies for implementing pedigree and track and trace solution for pharmaceutical and cosmetic products as recommended by FDA. ... - Mar 20
... June 2015 to July 2017 Pharma DSCSA Project Pharma DSCSA project is the application provided for pharmaceutical companies for implementing pedigree and track and trace solution for pharmaceutical and cosmetic products as recommended by FDA. ... - Mar 20
Senior Technical Writer
Morris Plains, NJ
... and foreign RRD regulatory to ensure compliance with FDA, INVIMA, and ANVISA submissions. ·Supported activities to maintain RRD product marketability in U.S. and foreign markets upon CMO change. ·Developed and fostered existing relationships with ... - Mar 15
... and foreign RRD regulatory to ensure compliance with FDA, INVIMA, and ANVISA submissions. ·Supported activities to maintain RRD product marketability in U.S. and foreign markets upon CMO change. ·Developed and fostered existing relationships with ... - Mar 15
Customer Service Account Manager
Ringwood, NJ
... from England.France,Italy,Portugal,Spain,Germany and Switzerland HACCP Certification Organic Certification Kosher Certificiation FDA liason USDA cheese licenses Achievement:Created product data base including nutrition,spec,sheets,sell sheets, label ... - Mar 14
... from England.France,Italy,Portugal,Spain,Germany and Switzerland HACCP Certification Organic Certification Kosher Certificiation FDA liason USDA cheese licenses Achievement:Created product data base including nutrition,spec,sheets,sell sheets, label ... - Mar 14
Program Management Gene Therapy
Wood Ridge, NJ
... company from Discovery through multiple IND approvals, IPO and M&A • Experience with implementing CMC strategies based on FDA/EMA guidance in Neurodegenerative and Pain diseases • Leader for technical teams in various departments including CMC, ... - Mar 11
... company from Discovery through multiple IND approvals, IPO and M&A • Experience with implementing CMC strategies based on FDA/EMA guidance in Neurodegenerative and Pain diseases • Leader for technical teams in various departments including CMC, ... - Mar 11
Clinical Research Associate
Belleville, NJ
... Possesses a profound understanding of ICH-GCP guidelines, FDA regulations, and ALCOA principles. Strong communication and ICT skills, combined with a meticulous eye for detail. THERAPEUTIC EXPERIENCE oMEDICAL DEVICES/IVD: Cardiovascular Devices, ... - Mar 08
... Possesses a profound understanding of ICH-GCP guidelines, FDA regulations, and ALCOA principles. Strong communication and ICT skills, combined with a meticulous eye for detail. THERAPEUTIC EXPERIENCE oMEDICAL DEVICES/IVD: Cardiovascular Devices, ... - Mar 08
Scientist
Mahwah, NJ
... • Authored and reviewed regulatory submission packages for IP, IB, Opt-In, IPA, and IND filings with the FDA. Evaluated support documentation for FDA and responded to questions from regulatory bodies • Crafted compelling presentations for higher ... - Mar 08
... • Authored and reviewed regulatory submission packages for IP, IB, Opt-In, IPA, and IND filings with the FDA. Evaluated support documentation for FDA and responded to questions from regulatory bodies • Crafted compelling presentations for higher ... - Mar 08
Customer Service Quality Assurance
Newark, NJ
... Verify that all entries we’re received from suppliers with required data and FDA release for customs audit regulations reports and graphs. Identify to which internal business the invoices/purchase order belonged to and provide data to the finance ... - Mar 05
... Verify that all entries we’re received from suppliers with required data and FDA release for customs audit regulations reports and graphs. Identify to which internal business the invoices/purchase order belonged to and provide data to the finance ... - Mar 05
Sql Server Fp A
Teaneck, NJ
... approved by “Federal Drug Administrator (FDA)” to be used in drug manufacturing process. b) Chemical Hazard Information System: Application to record and produce Chemical Safety Data Sheet (CSDS) in PDF format. c) developed & implemented several ... - Feb 23
... approved by “Federal Drug Administrator (FDA)” to be used in drug manufacturing process. b) Chemical Hazard Information System: Application to record and produce Chemical Safety Data Sheet (CSDS) in PDF format. c) developed & implemented several ... - Feb 23