| Resume alert | Resumes 61 - 70 of 648 |
Project Management Quality Assurance
Bound Brook, NJ
... • Developed and analyzed test scripts to ensure achievement of specified functionalities in compliance with 21CFR Part 11 rules set by FDA. • Built reports to summarize testing outcomes using Cognos 7.3 Series. • Spearheaded complete manual testing ... - 2023 Sep 07
... • Developed and analyzed test scripts to ensure achievement of specified functionalities in compliance with 21CFR Part 11 rules set by FDA. • Built reports to summarize testing outcomes using Cognos 7.3 Series. • Spearheaded complete manual testing ... - 2023 Sep 07
Data Entry Customer Service
Irvington, NJ
... Develop and maintain an excel spreadsheet or other mechanism to track corporate compliance Prepared procurement documentation including purchase orders, contracts and amendments Knowledge of cGMP/compliance/FDA Excellent organization and team ... - 2023 Sep 06
... Develop and maintain an excel spreadsheet or other mechanism to track corporate compliance Prepared procurement documentation including purchase orders, contracts and amendments Knowledge of cGMP/compliance/FDA Excellent organization and team ... - 2023 Sep 06
Quality Control C#
Whitehouse Station, NJ
... EuTech Scientific Services – Highland Park, NJ November 2018 to June 2021 Analytical Chemist Key Responsibilities and Achievements: Participate in FDA-regulated contract research services that emphasize innovating analytical methodologies for the ... - 2023 Aug 26
... EuTech Scientific Services – Highland Park, NJ November 2018 to June 2021 Analytical Chemist Key Responsibilities and Achievements: Participate in FDA-regulated contract research services that emphasize innovating analytical methodologies for the ... - 2023 Aug 26
Customer Service Accounts Payable
Newark, NJ
... ●Maintain GMP and cGMP compliance to meet regulatory requirements of the FDA. ●Document processes and SAP functionality – processes, flowcharts, procedures, work instructions, configurations. Support SAP Core Model ●Review master batch records, ... - 2023 Jul 27
... ●Maintain GMP and cGMP compliance to meet regulatory requirements of the FDA. ●Document processes and SAP functionality – processes, flowcharts, procedures, work instructions, configurations. Support SAP Core Model ●Review master batch records, ... - 2023 Jul 27
Data Entry Hearing Aid
Flanders, NJ, 07836
... Familiar with TJC, OSHA and FDA guidelines, quality team player with accuracy-focused and efficient approach, offering 6 years of industry expertise. Possess track record of contributing to increasing company sales helping audiologist on board. ... - 2023 Jul 21
... Familiar with TJC, OSHA and FDA guidelines, quality team player with accuracy-focused and efficient approach, offering 6 years of industry expertise. Possess track record of contributing to increasing company sales helping audiologist on board. ... - 2023 Jul 21
Clinical Research Quality Assurance
Green Knoll, NJ, 08807
... regulation compliance: DEA, FDA, Board of Pharmacy, Biohazard, Dept. of Health With consent & GCP collected specimens from patients; conducted experimentation, analyzed lab data; National Institute of Health grant proposal research submission; ... - 2023 Jul 21
... regulation compliance: DEA, FDA, Board of Pharmacy, Biohazard, Dept. of Health With consent & GCP collected specimens from patients; conducted experimentation, analyzed lab data; National Institute of Health grant proposal research submission; ... - 2023 Jul 21
Technical Program Manager
Edison, NJ
... • Led and precipitated in SOX Compliance audits, GXP Validation interview and audits, FDA regulations audits, Application Security reviews. • Developed strategic insights and digital products for the following industrial domains: Shipping ... - 2023 Jun 30
... • Led and precipitated in SOX Compliance audits, GXP Validation interview and audits, FDA regulations audits, Application Security reviews. • Developed strategic insights and digital products for the following industrial domains: Shipping ... - 2023 Jun 30
Quality Engineer Assurance Specialist
Paterson, NJ, 07505
... received from external customers with respect to business objectives and in compliance with Food and Drug Administration (FDA), International Standards Organization (ISO), Quality System Requirements (QSR), and other regulatory guidelines. ... - 2023 Jun 20
... received from external customers with respect to business objectives and in compliance with Food and Drug Administration (FDA), International Standards Organization (ISO), Quality System Requirements (QSR), and other regulatory guidelines. ... - 2023 Jun 20
Senior Supply Chain Management Leader
Warren, NJ
... • Guided launch activities for key product manufactured at external partner that led to FDA approval. Scientist, Pharmaceutical and Material Sciences (2010 – 2013) Senior Associate Scientist (2008 – 2009) Associate Scientist (2003 – 2007) Janssen ... - 2023 Jun 05
... • Guided launch activities for key product manufactured at external partner that led to FDA approval. Scientist, Pharmaceutical and Material Sciences (2010 – 2013) Senior Associate Scientist (2008 – 2009) Associate Scientist (2003 – 2007) Janssen ... - 2023 Jun 05
Documentation Specialist Tax Preparer
Iselin, NJ
... Review and approval of analysis reports/certificate of compliances for batches, stability studies, raw materials, and packaging component Implemented extensive changes to bring company with compliance with FDA and EPA. Assisted to retain the ... - 2023 Jun 01
... Review and approval of analysis reports/certificate of compliances for batches, stability studies, raw materials, and packaging component Implemented extensive changes to bring company with compliance with FDA and EPA. Assisted to retain the ... - 2023 Jun 01