| Resume alert | Resumes 21 - 30 of 626 |
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
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
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
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
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
... 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
Analytical Test Development
Piscataway, NJ
... Improved Quality Operation of team for GMP audit, FDA and Health Canada site inspection. Managed analysts training and performance using iShift and ADP. Scientist, QC Analytical Excellence Department (May 2021 – May 2022) Oversaw/ led ... - Jan 12
... Improved Quality Operation of team for GMP audit, FDA and Health Canada site inspection. Managed analysts training and performance using iShift and ADP. Scientist, QC Analytical Excellence Department (May 2021 – May 2022) Oversaw/ led ... - Jan 12