| Resume alert | Resumes 51 - 60 of 1181 |
Quality Control Regulatory Compliance
Caldwell, NJ
... Compliance professional in Fragrance and Flavor Industry .Strong analytical and technical knowledge Essential oils, Oleoresins,and Natural and Artificial Aroma compounds.Competent in FDA, FEMA, TTB and OSHA regulations of flavors and raw materials. ... - Jan 21
... Compliance professional in Fragrance and Flavor Industry .Strong analytical and technical knowledge Essential oils, Oleoresins,and Natural and Artificial Aroma compounds.Competent in FDA, FEMA, TTB and OSHA regulations of flavors and raw materials. ... - Jan 21
General Counsel Law Clerk
Chatham, NJ, 07928
... and Amgen Manufacturing Ltd., in response to clients’ submission to FDA of a license application for Amjevita® (adalimumab-atto) as a biosimilar to plaintiffs’ Humira® (adalimumab) reference product for treating multiple inflammatory diseases, ... - Jan 20
... and Amgen Manufacturing Ltd., in response to clients’ submission to FDA of a license application for Amjevita® (adalimumab-atto) as a biosimilar to plaintiffs’ Humira® (adalimumab) reference product for treating multiple inflammatory diseases, ... - Jan 20
Data Analyst Accounts Payable
Edison, NJ
... Sample products examine for FDA Validation of bulk & finished products manufactured by contractors prior to release. Performed the review and disposition of batch manufacturing and packaging records. Reviewed Certificates of Analysis and Compliance ... - Jan 18
... Sample products examine for FDA Validation of bulk & finished products manufactured by contractors prior to release. Performed the review and disposition of batch manufacturing and packaging records. Reviewed Certificates of Analysis and Compliance ... - Jan 18
Quality Assurance Regulatory Affairs
Irvington, NJ
... s production activities comply with government regulation SUMMARY OF TECHNICAL SKILLS High level of understanding of applicable regulations, including FDA (21CFR 312 and 314), ICH (E2A, E2B, E2C), GCP guidelines, EMA regulations, GVP Modules, etc. ... - Jan 15
... s production activities comply with government regulation SUMMARY OF TECHNICAL SKILLS High level of understanding of applicable regulations, including FDA (21CFR 312 and 314), ICH (E2A, E2B, E2C), GCP guidelines, EMA regulations, GVP Modules, etc. ... - Jan 15
Pharmacy Technician Customer Service
Carteret, NJ
... Skills: • MS Office • Pharmacy Calculations • Compounding medication following aseptic techniques • Injections • Sterile Preparations • Prescription Process • Drug Classification & Safety • Medicine Inventory • FDA Compliance • Customer Service ... - Jan 14
... Skills: • MS Office • Pharmacy Calculations • Compounding medication following aseptic techniques • Injections • Sterile Preparations • Prescription Process • Drug Classification & Safety • Medicine Inventory • FDA Compliance • Customer Service ... - Jan 14
Analytical Test Development
Piscataway, NJ
... Improved Quality Operation of team for GMP audit, FDA and Health Canada site inspection. Managed analysts training and performance using iShift and ADP. Scientist, QC Analytical Excellence Department (May 2021 – May 2022) Oversaw/ led ... - Jan 12
... Improved Quality Operation of team for GMP audit, FDA and Health Canada site inspection. Managed analysts training and performance using iShift and ADP. Scientist, QC Analytical Excellence Department (May 2021 – May 2022) Oversaw/ led ... - Jan 12
Clinical Research Senior
New York, NY
... • Supervised personnel in preparing timelines, SOPs, and ICF, and resolved deviations, adhering to FDA, ICH, and GCP guidelines. Clinical Data Associate DOCS Global, contracted with Abraham Cancer Center, University of Pennsylvania, Philadelphia, PA ... - Jan 12
... • Supervised personnel in preparing timelines, SOPs, and ICF, and resolved deviations, adhering to FDA, ICH, and GCP guidelines. Clinical Data Associate DOCS Global, contracted with Abraham Cancer Center, University of Pennsylvania, Philadelphia, PA ... - Jan 12
Customer Service Pharmacy Technician
North Bergen, NJ
... skills Manual and automated medication dispensing Updating medication histories Prepare bubble packs Typing medication labels FDA Drug Safety Guidelines Speak Korean and English Fast learn everything and very patient listening well from others and ... - Jan 11
... skills Manual and automated medication dispensing Updating medication histories Prepare bubble packs Typing medication labels FDA Drug Safety Guidelines Speak Korean and English Fast learn everything and very patient listening well from others and ... - Jan 11
Quality Control Machine Operator
Elizabeth, NJ
... • Manufacturing (9 years) • Food Production (10+ years) • OSHA,PPE, FDA,SOP, Table Press (5 years) • Lean Manufacturing • Assembly • Leadership • Quality control • Continuous improvement • Team management • Single Punch Table Press, Pill Press. ... - Jan 09
... • Manufacturing (9 years) • Food Production (10+ years) • OSHA,PPE, FDA,SOP, Table Press (5 years) • Lean Manufacturing • Assembly • Leadership • Quality control • Continuous improvement • Team management • Single Punch Table Press, Pill Press. ... - Jan 09
Clinical Research Data Management
Teaneck, NJ
... 2023 Clinical Research Training covering Core Competencies including: ICH GCP E6 R (2) FDA Regulations 21CFR 11, 50, 54, 56 and the Common Rule 45CFR46 Data Management Informed Consent Process Clinical Trial Operations from feasibility through close ... - Jan 08
... 2023 Clinical Research Training covering Core Competencies including: ICH GCP E6 R (2) FDA Regulations 21CFR 11, 50, 54, 56 and the Common Rule 45CFR46 Data Management Informed Consent Process Clinical Trial Operations from feasibility through close ... - Jan 08