| Resume alert | Resumes 51 - 60 of 1416 |
Medical Reviewer Drug Safety
Edison, NJ
... Well versed with regulations related to prescribed products and medical devices and current with the regulatory requirements and expectations including EMA ICH GVP Modules, FDA IND and NDA reporting requirements and global risk management ... - Feb 09
... Well versed with regulations related to prescribed products and medical devices and current with the regulatory requirements and expectations including EMA ICH GVP Modules, FDA IND and NDA reporting requirements and global risk management ... - Feb 09
CUSTOMS ENTRY WRITER
Roselle Park, NJ
... commodities and multiple lines -Upon filling Entry provide release details to LFD (3461 and ACE results) -Advise OGA status, FDA or Agriculture holds or releases -Upload supporting documentation via DIS or ITACS -File CF-7512/IT In-Bond and arrive ... - Feb 09
... commodities and multiple lines -Upon filling Entry provide release details to LFD (3461 and ACE results) -Advise OGA status, FDA or Agriculture holds or releases -Upload supporting documentation via DIS or ITACS -File CF-7512/IT In-Bond and arrive ... - Feb 09
Project Management Program Manager
New York, NY
... ● Use QMS system to help create, edit, and track FDA required project documents. SEQUENT SOFTWARE/ Santa Clara, CA 2012–2023 Senior Program Manager and VP Customer Success (2019–2023) As a program and success executive with responsibilities for ... - Feb 09
... ● Use QMS system to help create, edit, and track FDA required project documents. SEQUENT SOFTWARE/ Santa Clara, CA 2012–2023 Senior Program Manager and VP Customer Success (2019–2023) As a program and success executive with responsibilities for ... - Feb 09
Vice President Compliance Officer
Ramsey, NJ
... CEO of RCS – Regulatory Compliance Services (a division of DIVA Pharmaceuticals) (Prime vendor for NJMEP and United Nations for over 20 years) • Developed third acceptable submission for FDA Approval for Cannabis Rx Drug. • Major interaction with ... - Feb 01
... CEO of RCS – Regulatory Compliance Services (a division of DIVA Pharmaceuticals) (Prime vendor for NJMEP and United Nations for over 20 years) • Developed third acceptable submission for FDA Approval for Cannabis Rx Drug. • Major interaction with ... - Feb 01
Medical Director Clinical Trial
West Orange, NJ
... The Dunn Group, Totowa, NJ 6/23 Complete 360 Competitive Intelligence analysis including assessment of current and future medical value/need and Financial ROI focused on roll-out strategy, and marketing plans for a new FDA approved post M.I. cardio ... - Jan 31
... The Dunn Group, Totowa, NJ 6/23 Complete 360 Competitive Intelligence analysis including assessment of current and future medical value/need and Financial ROI focused on roll-out strategy, and marketing plans for a new FDA approved post M.I. cardio ... - Jan 31
Business Analyst Supply Chain
Jersey City, NJ
... Knowledgeable with HIPAA, PHI, FDA, FISMA, ACA, GDPA, and claims from the purpose of entry of settling, claim review, recognizing claims preparing issues, their source, and giving prompt relating answers for their related emerging issues. HITECH ... - Jan 23
... Knowledgeable with HIPAA, PHI, FDA, FISMA, ACA, GDPA, and claims from the purpose of entry of settling, claim review, recognizing claims preparing issues, their source, and giving prompt relating answers for their related emerging issues. HITECH ... - Jan 23
Quality Control Regulatory Compliance
Caldwell, NJ
... Compliance professional in Fragrance and Flavor Industry .Strong analytical and technical knowledge Essential oils, Oleoresins,and Natural and Artificial Aroma compounds.Competent in FDA, FEMA, TTB and OSHA regulations of flavors and raw materials. ... - Jan 21
... Compliance professional in Fragrance and Flavor Industry .Strong analytical and technical knowledge Essential oils, Oleoresins,and Natural and Artificial Aroma compounds.Competent in FDA, FEMA, TTB and OSHA regulations of flavors and raw materials. ... - Jan 21
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
Data Analyst Accounts Payable
Edison, NJ
... Sample products examine for FDA Validation of bulk & finished products manufactured by contractors prior to release. Performed the review and disposition of batch manufacturing and packaging records. Reviewed Certificates of Analysis and Compliance ... - Jan 18
... Sample products examine for FDA Validation of bulk & finished products manufactured by contractors prior to release. Performed the review and disposition of batch manufacturing and packaging records. Reviewed Certificates of Analysis and Compliance ... - Jan 18
Creative Director Lung Cancer
Brooklyn, NY
... Emails and banners for Retevmo (an FDA approved treatment for Non-Small Cell Lung Cancer by Eli Lilly and Company). Digitas Health - Pitch work for Endo Aesthetics* (a new treatment for cellulite). Estee Lauder - Developed campaigns for Clinique, ... - Jan 17
... Emails and banners for Retevmo (an FDA approved treatment for Non-Small Cell Lung Cancer by Eli Lilly and Company). Digitas Health - Pitch work for Endo Aesthetics* (a new treatment for cellulite). Estee Lauder - Developed campaigns for Clinique, ... - Jan 17