| Resume alert | Resumes 51 - 60 of 611 |
Low Voltage Industrial Maintenance
Edison, NJ
... I understand the rigors of not only performing a task/project correctly but also documenting work in a fashion that is clear and concise since it is subject to FDA inspections. Realize the critical importance of developing relationships both inside ... - 2023 Dec 20
... I understand the rigors of not only performing a task/project correctly but also documenting work in a fashion that is clear and concise since it is subject to FDA inspections. Realize the critical importance of developing relationships both inside ... - 2023 Dec 20
Quality Assurance Control
Princeton, NJ, 08540
... Share point, LMS, MES PAS/X, Veeva Vault CDOCs, eDMS/EDC, Maximo, Microsoft office, Adobe Acrobat and DocuSign Knowledge of FDA regulations, 21 CFR 210 & 211, ICH guidelines, 21 CFR Part 11, ISO 9001, eTMF (electronic Trail Master File), eCRF, ... - 2023 Dec 14
... Share point, LMS, MES PAS/X, Veeva Vault CDOCs, eDMS/EDC, Maximo, Microsoft office, Adobe Acrobat and DocuSign Knowledge of FDA regulations, 21 CFR 210 & 211, ICH guidelines, 21 CFR Part 11, ISO 9001, eTMF (electronic Trail Master File), eCRF, ... - 2023 Dec 14
Quality Assurance Control
Trenton, NJ
... Verify the certificate of analysis and FDA documents for imported materials. Approve or reject the incoming candies and packaging material in M3 system. To supervise packaging room to assure packaging is done according to SOP. Perform metal detector ... - 2023 Dec 11
... Verify the certificate of analysis and FDA documents for imported materials. Approve or reject the incoming candies and packaging material in M3 system. To supervise packaging room to assure packaging is done according to SOP. Perform metal detector ... - 2023 Dec 11
Human Resources Manager
Middlesex, NJ
... and guidelines under the Good Clinical Practices (GCP), Standard Operating Procedures (SOPs), Federal Drug Administration (FDA) and International Conference on Harmonization (ICH) Suggest recommendations for changes to contracts, budgets, rental ... - 2023 Dec 08
... and guidelines under the Good Clinical Practices (GCP), Standard Operating Procedures (SOPs), Federal Drug Administration (FDA) and International Conference on Harmonization (ICH) Suggest recommendations for changes to contracts, budgets, rental ... - 2023 Dec 08
Quality Control Specialist
Somerset, NJ, 08873
... Knowledge of GMP, ISO, and FDA regulations and audit Experience with environmental monitoring, air and water sampling with GMP regulations. Performed Cross Functional Lab audits for FDA Inspection. Worked according to the approved validation ... - 2023 Dec 07
... Knowledge of GMP, ISO, and FDA regulations and audit Experience with environmental monitoring, air and water sampling with GMP regulations. Performed Cross Functional Lab audits for FDA Inspection. Worked according to the approved validation ... - 2023 Dec 07
Customer Service Account Executive
Newtown, PA
... VP, National Accounts, Eurand Pharmaceuticals, Milan, Italy/Yardley, PA 4/2009 - 5/2011 Responsible for a start-up company, with the launch of FDA approved products into the US. Sales from $0 to $145M first year, Exceeding fist year expectations by ... - 2023 Dec 03
... VP, National Accounts, Eurand Pharmaceuticals, Milan, Italy/Yardley, PA 4/2009 - 5/2011 Responsible for a start-up company, with the launch of FDA approved products into the US. Sales from $0 to $145M first year, Exceeding fist year expectations by ... - 2023 Dec 03
Project Management Senior Manager
Fairless Hills, PA
... by 15% and healthcare membership initiatives by 9% Conducted market research & identified solutions to challenges faced by FDA regulations for external stakeholders SENIOR REGIONAL MARKETING MANAGER, 2008 to 2012 DOW JONES & COMPANY, South ... - 2023 Nov 29
... by 15% and healthcare membership initiatives by 9% Conducted market research & identified solutions to challenges faced by FDA regulations for external stakeholders SENIOR REGIONAL MARKETING MANAGER, 2008 to 2012 DOW JONES & COMPANY, South ... - 2023 Nov 29
Supply Chain Associate Director
Dayton, NJ
... • Planned Equipment & Time Constraints • Performance Reporting & Updates • International Regulations & Customs • Import/Export & FDA/DEA Experience • Proactive & Responsive Customer Service • Excellent Verbal & Written Communication Work Experience ... - 2023 Nov 27
... • Planned Equipment & Time Constraints • Performance Reporting & Updates • International Regulations & Customs • Import/Export & FDA/DEA Experience • Proactive & Responsive Customer Service • Excellent Verbal & Written Communication Work Experience ... - 2023 Nov 27
CSV Specialist, Compliance Specialist, Quality Control and AR&D Lab
Hillsborough, NJ
... Department • 2 years of GMP quality compliance/quality assurance experience • Extensive knowledge of GAMP 5, ICH Guidance, FDA regulations including CSA (draft), EU Annex, MHRA, and OECD Guidelines, FDA’s Pre-Approval Inspection (PAI) Program • ... - 2023 Nov 17
... Department • 2 years of GMP quality compliance/quality assurance experience • Extensive knowledge of GAMP 5, ICH Guidance, FDA regulations including CSA (draft), EU Annex, MHRA, and OECD Guidelines, FDA’s Pre-Approval Inspection (PAI) Program • ... - 2023 Nov 17
Quality Assurance Business Development
Somerset, NJ
... Broad knowledge of Environmental monitoring, microbiology, Regulatory submissions including IND, ANDA and NDA, Annual Product Review, Process Validation: GxP, cGMP, cGLP, cGCP, GDP, FDA, ANVISA and MHRA regulations, DEA, EMA, USP, EP and ICH ... - 2023 Nov 16
... Broad knowledge of Environmental monitoring, microbiology, Regulatory submissions including IND, ANDA and NDA, Annual Product Review, Process Validation: GxP, cGMP, cGLP, cGCP, GDP, FDA, ANVISA and MHRA regulations, DEA, EMA, USP, EP and ICH ... - 2023 Nov 16