| Resume alert | Resumes 1 - 10 of 290 |
Information Technology Supply Chain
Morristown, NJ
... Strong understanding of IT Governance (SOX ITGC) for FDA and global/global regulatory audits. Excellent interpersonal skills to manage multiple priorities in a dynamic environment. Experience in ITSM tools such as ServiceNow to manage global ... - Apr 22
... Strong understanding of IT Governance (SOX ITGC) for FDA and global/global regulatory audits. Excellent interpersonal skills to manage multiple priorities in a dynamic environment. Experience in ITSM tools such as ServiceNow to manage global ... - Apr 22
Supply Chain Senior Director
Hopatcong, NJ
... Supply Chain FDA inspection subject matter expert. • Created and optimized scheduling methodology for an immunotherapy product line. • Responsible for the development and maintenance of production schedules for both commercial and clinical products. ... - Apr 21
... Supply Chain FDA inspection subject matter expert. • Created and optimized scheduling methodology for an immunotherapy product line. • Responsible for the development and maintenance of production schedules for both commercial and clinical products. ... - Apr 21
Project Manager Change Management
Bridgewater, NJ
... Developed online Learning Management System (LMS) for certification process training and to meet FDA / compliance requirements. Provided guidance on change management methodology and related communications for stakeholder and user clarity. Ricoh ... - Mar 26
... Developed online Learning Management System (LMS) for certification process training and to meet FDA / compliance requirements. Provided guidance on change management methodology and related communications for stakeholder and user clarity. Ricoh ... - Mar 26
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
Pharmacy Technician Prior Authorization
Warren, NJ
... Khan, MBCS Cell: 201-***-**** Email: ad38vr@r.postjobfree.com Skills US PQC, PTC, FDA, GMID, LMID, GPV, Siebel (ACES), Trackwise, NICE, 21 CFR820, 803, ISO 13485. EUMDR. Veeva Vault, Micro Merchant, Prime Rx, Comet, Pfizer Compliance Education ... - Mar 10
... Khan, MBCS Cell: 201-***-**** Email: ad38vr@r.postjobfree.com Skills US PQC, PTC, FDA, GMID, LMID, GPV, Siebel (ACES), Trackwise, NICE, 21 CFR820, 803, ISO 13485. EUMDR. Veeva Vault, Micro Merchant, Prime Rx, Comet, Pfizer Compliance Education ... - Mar 10
United States Materials Handler
Raritan, NJ
... sap knowledge October 2021-February 2022 Materials Handler Ortho-Clinical Diagnostics Raritan, New Jersey, United States Safely and accurately process Customer products according to established procedures within FDA, ISO, and GMP guidelines. ship ... - Mar 01
... sap knowledge October 2021-February 2022 Materials Handler Ortho-Clinical Diagnostics Raritan, New Jersey, United States Safely and accurately process Customer products according to established procedures within FDA, ISO, and GMP guidelines. ship ... - Mar 01
Project Manager Business Development
Millington, NJ
... Handled real-time online inventory and payment management (UI, UX, ERP), created communication channels, branding specific to consumer needs, managed FDA regulations pertaining to safety of the products and fair packaging and labeling, handled GXP ... - Feb 29
... Handled real-time online inventory and payment management (UI, UX, ERP), created communication channels, branding specific to consumer needs, managed FDA regulations pertaining to safety of the products and fair packaging and labeling, handled GXP ... - Feb 29
Regulatory Affairs Project Management
Bridgewater, NJ
JEAN HALLORAN 908-***-**** (Cell) ad3q98@r.postjobfree.com PROFESSIONAL SUMMARY Experienced and dedicated Regulatory Professional with over sixteen years of Regulatory experience in the pharmaceutical industry with a strong focus on FDA Submissions. ... - Feb 19
JEAN HALLORAN 908-***-**** (Cell) ad3q98@r.postjobfree.com PROFESSIONAL SUMMARY Experienced and dedicated Regulatory Professional with over sixteen years of Regulatory experience in the pharmaceutical industry with a strong focus on FDA Submissions. ... - Feb 19
Support Team Customer Service
Rockaway, NJ
... Documented training according to all regulations and standards including FDA 21CFR820 and ISO 13485. Freelance IT Admin, Miami, FL - PC Technician and IT Support (05/2003 - 01/2012) ●Designed and built custom PCs and networking setups based on the ... - Feb 09
... Documented training according to all regulations and standards including FDA 21CFR820 and ISO 13485. Freelance IT Admin, Miami, FL - PC Technician and IT Support (05/2003 - 01/2012) ●Designed and built custom PCs and networking setups based on the ... - Feb 09
General Counsel Law Clerk
Chatham, NJ, 07928
... and Amgen Manufacturing Ltd., in response to clients’ submission to FDA of a license application for Amjevita® (adalimumab-atto) as a biosimilar to plaintiffs’ Humira® (adalimumab) reference product for treating multiple inflammatory diseases, ... - Jan 20
... and Amgen Manufacturing Ltd., in response to clients’ submission to FDA of a license application for Amjevita® (adalimumab-atto) as a biosimilar to plaintiffs’ Humira® (adalimumab) reference product for treating multiple inflammatory diseases, ... - Jan 20