| Resume alert | Resumes 21 - 30 of 977 |
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
Clinical Research Associate
Belleville, NJ
... Possesses a profound understanding of ICH-GCP guidelines, FDA regulations, and ALCOA principles. Strong communication and ICT skills, combined with a meticulous eye for detail. THERAPEUTIC EXPERIENCE oMEDICAL DEVICES/IVD: Cardiovascular Devices, ... - Mar 08
... Possesses a profound understanding of ICH-GCP guidelines, FDA regulations, and ALCOA principles. Strong communication and ICT skills, combined with a meticulous eye for detail. THERAPEUTIC EXPERIENCE oMEDICAL DEVICES/IVD: Cardiovascular Devices, ... - Mar 08
Clinical drug trials, pharmacovigilance, certified in human research
Edison, NJ, 08817
... ●Decreased possible late cases through root cause analysis of non-compliant single case reports, circumventing FDA audits and fines, resulting in significant overall savings. Drug Safety Associate Consultant Experience: G & W Laboratories Inc., ... - Mar 06
... ●Decreased possible late cases through root cause analysis of non-compliant single case reports, circumventing FDA audits and fines, resulting in significant overall savings. Drug Safety Associate Consultant Experience: G & W Laboratories Inc., ... - Mar 06
Customer Service Quality Assurance
Newark, NJ
... Verify that all entries we’re received from suppliers with required data and FDA release for customs audit regulations reports and graphs. Identify to which internal business the invoices/purchase order belonged to and provide data to the finance ... - Mar 05
... Verify that all entries we’re received from suppliers with required data and FDA release for customs audit regulations reports and graphs. Identify to which internal business the invoices/purchase order belonged to and provide data to the finance ... - Mar 05
Patient Care Nurse Coordinator
Clark, NJ, 07066
... WORD/EXCEL ●ONS CERTIFIED ●IND SAFETY REPORTING ●EPIC HYPERSPACE SYSTEM ●FLUENT IN SPANISH ●WIRB/IRB SAFETY REPORTING ●FDA EXPERIENCE WITH MULTIPLE SUCCESSFUL AUDITS ●CCRP ●CONFERENCE ATTENDANCE, INCLUDING ASH TRIALS PARTICIPATED IN THAT LEAD ... - Mar 03
... WORD/EXCEL ●ONS CERTIFIED ●IND SAFETY REPORTING ●EPIC HYPERSPACE SYSTEM ●FLUENT IN SPANISH ●WIRB/IRB SAFETY REPORTING ●FDA EXPERIENCE WITH MULTIPLE SUCCESSFUL AUDITS ●CCRP ●CONFERENCE ATTENDANCE, INCLUDING ASH TRIALS PARTICIPATED IN THAT LEAD ... - Mar 03
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
Project Management Business Analyst
East Brunswick, NJ
... • Conducted assays and test methods according to 21 CFR and FDA guidelines, including ELISA, BCA (colorimetric assay), LAL endotoxin, SDS-PAGE, and cell culture technique TLR-5 assay (in training). BRISTOL MYERS SQUIBB, Plainsboro, NJ 2004 - 2009 ... - Feb 28
... • Conducted assays and test methods according to 21 CFR and FDA guidelines, including ELISA, BCA (colorimetric assay), LAL endotoxin, SDS-PAGE, and cell culture technique TLR-5 assay (in training). BRISTOL MYERS SQUIBB, Plainsboro, NJ 2004 - 2009 ... - Feb 28
Raw Materials Quality Control
Marlboro, NJ
... Work in heavily FDA regulated cGMP environment and follow lab procedures. Performing adjustment to the in-process batches by calculations when there is out of specification result. Maintain accurate documentation of test results. Enter test results ... - Feb 24
... Work in heavily FDA regulated cGMP environment and follow lab procedures. Performing adjustment to the in-process batches by calculations when there is out of specification result. Maintain accurate documentation of test results. Enter test results ... - Feb 24