| Resume alert | Resumes 41 - 50 of 1475 |
Art Director Social Media
New York, NY
... FREELANCE ASSOCIATE CREATIVE DIRECTOR, New York, NY VML, HELLER, DEFY, AREA 23, NEON HEALTH, DDB HEALTH, DUZIE FASHION, SKINSHINEBAR, HERITAGE INDIA FASHIONS KEY ACHIEVEMENTS: Designed and launched websites as well as the first FDA approved medical ... - Feb 16
... FREELANCE ASSOCIATE CREATIVE DIRECTOR, New York, NY VML, HELLER, DEFY, AREA 23, NEON HEALTH, DDB HEALTH, DUZIE FASHION, SKINSHINEBAR, HERITAGE INDIA FASHIONS KEY ACHIEVEMENTS: Designed and launched websites as well as the first FDA approved medical ... - Feb 16
Pharmacist
Queens, NY
... with Mary Ann Howland Formal Letter addressed to: FDA (Food and Drug Administration) SKILLS Languages: English (Native), Bengali (intermediate), Spanish (Beginner) Technical Skills: Microsoft Office, EPIC, Pyxis, Scriptpath Rx, Citrix, Biotrack - Feb 14
... with Mary Ann Howland Formal Letter addressed to: FDA (Food and Drug Administration) SKILLS Languages: English (Native), Bengali (intermediate), Spanish (Beginner) Technical Skills: Microsoft Office, EPIC, Pyxis, Scriptpath Rx, Citrix, Biotrack - Feb 14
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
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
Quality Assurance Control/Production Management
Parlin, NJ
... * Reviewed and approved Batch documentations for FDA regulated products. * Document control coordinator for the organization, keeping track of procedures and their lifecycle, issue new procedures and archive old when no longer needed. * Setup ... - Feb 06
... * Reviewed and approved Batch documentations for FDA regulated products. * Document control coordinator for the organization, keeping track of procedures and their lifecycle, issue new procedures and archive old when no longer needed. * Setup ... - Feb 06
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