| Resume alert | Resumes 21 - 30 of 648 |
Human Resources Patient Care
Edison, NJ
... Clinical Quality Program Standards Drug Utilization Review Medication Therapy Management Medicare and Medicaid Processes FDA Drug Safety Guidelines and SOP for operations Soft Skills: Detail-oriented, time management, collaborative, teamwork, ... - Feb 19
... Clinical Quality Program Standards Drug Utilization Review Medication Therapy Management Medicare and Medicaid Processes FDA Drug Safety Guidelines and SOP for operations Soft Skills: Detail-oriented, time management, collaborative, teamwork, ... - Feb 19
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
Software Development Management Process
Edison, NJ
... Compliance – Ensured compliance with all CCT standards, SOX, FDA, GXP, CSV, 21 CFR part 11, SDLC, SOP and other regulatory requirements. Celgene Inc. – Summit, NJ (http://www.celgene.com) IT Consultant February 2005 – April 2006 IT Projects – ... - Feb 17
... Compliance – Ensured compliance with all CCT standards, SOX, FDA, GXP, CSV, 21 CFR part 11, SDLC, SOP and other regulatory requirements. Celgene Inc. – Summit, NJ (http://www.celgene.com) IT Consultant February 2005 – April 2006 IT Projects – ... - Feb 17
United States Quality Control
Wayne, NJ
... Control Printed Circuit Board (PCB) Voltmeter Safety Standards Blueprints Machine Tool Documentation Process Improvement Metrics FDA (Food and Drug Administration) Problem Solving Skills Standard Operating Procedures (SOP) Performance Analysis ... - Feb 13
... Control Printed Circuit Board (PCB) Voltmeter Safety Standards Blueprints Machine Tool Documentation Process Improvement Metrics FDA (Food and Drug Administration) Problem Solving Skills Standard Operating Procedures (SOP) Performance Analysis ... - Feb 13
Project Manager Senior
Wyckoff, NJ, 07481
... ● Ensured every step of the intense graphics process was met, to ensure compliance with FDA, EUMDR and IVDR mandates from each country for audit trail. ● Worked with the Translation and Content Department to acquire translated copy for each ... - Feb 11
... ● Ensured every step of the intense graphics process was met, to ensure compliance with FDA, EUMDR and IVDR mandates from each country for audit trail. ● Worked with the Translation and Content Department to acquire translated copy for each ... - Feb 11
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
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
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
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
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