| Resume alert | Resumes 21 - 30 of 962 |
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
Quality Assurance Control
Jersey City, NJ
... of quality parameters during production (filling, crimping ) • Inspection of packaging procedures (labeling, packaging quality, ...) • Set up Packaging and production equipments In Quality Assurance • Solid knowledge of Health Canada and FDA GMPs. ... - Feb 22
... of quality parameters during production (filling, crimping ) • Inspection of packaging procedures (labeling, packaging quality, ...) • Set up Packaging and production equipments In Quality Assurance • Solid knowledge of Health Canada and FDA GMPs. ... - Feb 22
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
Computer System Validation
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 21
... 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 21
Human Resources Patient Care
Edison, NJ
... Clinical Quality Program Standards Drug Utilization Review Medication Therapy Management Medicare and Medicaid Processes FDA Drug Safety Guidelines and SOP for operations Soft Skills: Detail-oriented, time management, collaborative, teamwork, ... - Feb 19
... Clinical Quality Program Standards Drug Utilization Review Medication Therapy Management Medicare and Medicaid Processes FDA Drug Safety Guidelines and SOP for operations Soft Skills: Detail-oriented, time management, collaborative, teamwork, ... - Feb 19
Regulatory Affairs Project Management
Bridgewater, NJ
JEAN HALLORAN 908-***-**** (Cell) ad3q98@r.postjobfree.com PROFESSIONAL SUMMARY Experienced and dedicated Regulatory Professional with over sixteen years of Regulatory experience in the pharmaceutical industry with a strong focus on FDA Submissions. ... - Feb 19
JEAN HALLORAN 908-***-**** (Cell) ad3q98@r.postjobfree.com PROFESSIONAL SUMMARY Experienced and dedicated Regulatory Professional with over sixteen years of Regulatory experience in the pharmaceutical industry with a strong focus on FDA Submissions. ... - Feb 19