| Resume alert | Resumes 11 - 20 of 710 |
Remediation Admin Training Specialist
Tinton Falls, NJ
... review training administration procedures to ensure alignment with current site initiatives, regulatory body requirements (FDA, DEKRA, and AATB) and Global Corporate training procedures Develop criteria to evaluate the effectiveness of training ... - Mar 25
... review training administration procedures to ensure alignment with current site initiatives, regulatory body requirements (FDA, DEKRA, and AATB) and Global Corporate training procedures Develop criteria to evaluate the effectiveness of training ... - Mar 25
Quality Assurance Project Management
North Brunswick, NJ
... Document Management System), SAP(System Applications products in Data Processing) - Provide all necessary documents to FDA, visitors and auditors by putting uncontrolled copies stamp - To maintain all inventories required for documentation. ... - Mar 17
... Document Management System), SAP(System Applications products in Data Processing) - Provide all necessary documents to FDA, visitors and auditors by putting uncontrolled copies stamp - To maintain all inventories required for documentation. ... - Mar 17
16+ years in Pharmacovigilance. Phase I clinical drug trials as a RN
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 15
... 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 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 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
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 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
Quality analyst
Lakewood, NJ, 08701
... College Computer science Professional Experience 2022/01 – 2024/01 Quality Analyst -Batch Specialist Life Science Labs •Conducted batches reconciliation, involving precise math calculations to ensure adherence to GMP regulations and FDA guidance. ... - Feb 28
... College Computer science Professional Experience 2022/01 – 2024/01 Quality Analyst -Batch Specialist Life Science Labs •Conducted batches reconciliation, involving precise math calculations to ensure adherence to GMP regulations and FDA guidance. ... - 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
Qa Lead Computer System
Edison, NJ
... Evaluates validation activities and documentation to ensure that they meet FDA standards, User Requirements, deliverables such as Validation Plan, Test Plan Protocols, Validation Summery report, Risk Assessments Reports, Experience in generating, ... - Feb 22
... Evaluates validation activities and documentation to ensure that they meet FDA standards, User Requirements, deliverables such as Validation Plan, Test Plan Protocols, Validation Summery report, Risk Assessments Reports, Experience in generating, ... - Feb 22