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FDA resumes in Parsippany, NJ

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Resume alert Resumes 21 - 30 of 1181

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

Customer Service Account Manager

Ringwood, NJ
... from England.France,Italy,Portugal,Spain,Germany and Switzerland HACCP Certification Organic Certification Kosher Certificiation FDA liason USDA cheese licenses Achievement:Created product data base including nutrition,spec,sheets,sell sheets, label ... - Mar 14

Program Management Gene Therapy

Wood Ridge, NJ
... company from Discovery through multiple IND approvals, IPO and M&A • Experience with implementing CMC strategies based on FDA/EMA guidance in Neurodegenerative and Pain diseases • Leader for technical teams in various departments including CMC, ... - Mar 11

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

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

Scientist

Mahwah, NJ
... • Authored and reviewed regulatory submission packages for IP, IB, Opt-In, IPA, and IND filings with the FDA. Evaluated support documentation for FDA and responded to questions from regulatory bodies • Crafted compelling presentations for higher ... - 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

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

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

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
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