| Resume alert | Resumes 61 - 70 of 395 |
QA Associate II
Monroe Township, NJ, 08831
... Review cell/gene therapy raw data generated utilizing ELISA, plate reader and Soft Max Pro (GLP &GMP) Evaluate data and audit trails generated utilizing analytical tools such as HPLC, UPLC, GC, LC/MS, ICP-MS, XRD, Dissolution, Titration, etc. ... - 2023 Jun 22
... Review cell/gene therapy raw data generated utilizing ELISA, plate reader and Soft Max Pro (GLP &GMP) Evaluate data and audit trails generated utilizing analytical tools such as HPLC, UPLC, GC, LC/MS, ICP-MS, XRD, Dissolution, Titration, etc. ... - 2023 Jun 22
Processing Technician Warehouse Employee
Roosevelt, NJ, 08555
... 10+ years of GMP manufacturing experience. Muscular Skeletal Transplant Foundation M.T.F – Edison, NJ July 2011 – January 2022 Dermis Master Processing Technician/Trainer, MTF November 2018 – January 2022 Perform Aseptic process of Dermal layers, ... - 2023 Jun 09
... 10+ years of GMP manufacturing experience. Muscular Skeletal Transplant Foundation M.T.F – Edison, NJ July 2011 – January 2022 Dermis Master Processing Technician/Trainer, MTF November 2018 – January 2022 Perform Aseptic process of Dermal layers, ... - 2023 Jun 09
Quality Manager Project
Monroe Township, NJ
... Superior understanding of GAMP, GxPs (GCP, GLP, and GMP), and the Electronic Records, Electronic Signatures, and Audit Trails regulations found in 21-CFR Part 11. Expertise in developing and revising User Requirement Specifications (URS), Functional ... - 2023 Jun 05
... Superior understanding of GAMP, GxPs (GCP, GLP, and GMP), and the Electronic Records, Electronic Signatures, and Audit Trails regulations found in 21-CFR Part 11. Expertise in developing and revising User Requirement Specifications (URS), Functional ... - 2023 Jun 05
Documentation Specialist Tax Preparer
Iselin, NJ
... Newark, NJ March 2022 – November 2022 QA Specialist: Writing, revising, review of SOPs, Batch Records Review and Release, Daily monitoring GMP compliances, Maintained Retain Samples rooms for stability studies, Maintained data base for QA ... - 2023 Jun 01
... Newark, NJ March 2022 – November 2022 QA Specialist: Writing, revising, review of SOPs, Batch Records Review and Release, Daily monitoring GMP compliances, Maintained Retain Samples rooms for stability studies, Maintained data base for QA ... - 2023 Jun 01
Material Handler Production Operator
Edison, NJ
... Amneal Pharmaceutical, Branchburg, NJ February2023-Present Production Operator II ● Machine operator ● Follow SOPs, QSR, and GMP per Instructions and Production Records paper works ● Reading and quality check of manufacturing products and maintain ... - 2023 May 31
... Amneal Pharmaceutical, Branchburg, NJ February2023-Present Production Operator II ● Machine operator ● Follow SOPs, QSR, and GMP per Instructions and Production Records paper works ● Reading and quality check of manufacturing products and maintain ... - 2023 May 31
Manufacturing Associate Production
Newtown, PA
... Works with Validation and leads process, equipment, and cleaning validation initiatives within the GMP facility as needed Supports validation efforts associated with manufacturing equipment and processes Reviews batch records and logbooks Provide ... - 2023 May 30
... Works with Validation and leads process, equipment, and cleaning validation initiatives within the GMP facility as needed Supports validation efforts associated with manufacturing equipment and processes Reviews batch records and logbooks Provide ... - 2023 May 30
Facilities Manager
Franklin Park, NJ, 08823
... Worked with facility manager who handled routine facility management operations, including GXP, GMP, procurement of supplies and services, issued purchase orders, managed bid requests and construction contracts and processed accounts payable and ... - 2023 May 23
... Worked with facility manager who handled routine facility management operations, including GXP, GMP, procurement of supplies and services, issued purchase orders, managed bid requests and construction contracts and processed accounts payable and ... - 2023 May 23
Technical Writer Regulatory Affairs
Ewing, NJ, 08618
... Edit/Write a variety of technical articles, reports, manuals, flow charts and other documentation for a wide range of uses, including GMP operations and validation activities. Assist in assembly of validation package documents for GMP libraries. ... - 2023 May 19
... Edit/Write a variety of technical articles, reports, manuals, flow charts and other documentation for a wide range of uses, including GMP operations and validation activities. Assist in assembly of validation package documents for GMP libraries. ... - 2023 May 19
Packaging Associate Machine
Hillsborough, NJ
... ● Responsible for accurately maintaining legible and accurate records, required logs, books, records, and other procedures to comply with regulatory requirements, Good Manufacturing Practices (GMP), Quality Systems Regulations, Standard Operating ... - 2023 May 14
... ● Responsible for accurately maintaining legible and accurate records, required logs, books, records, and other procedures to comply with regulatory requirements, Good Manufacturing Practices (GMP), Quality Systems Regulations, Standard Operating ... - 2023 May 14
Laboratory Technician Sales Coordinator
Colonia, NJ
... Excellent working knowledge of GMP, and OSHA requirement. Hardworking, reliable, and flexible; willing to work long hours and additional shift to complete a project. Complete assignments under minimal supervision; work well independently and as team ... - 2023 May 01
... Excellent working knowledge of GMP, and OSHA requirement. Hardworking, reliable, and flexible; willing to work long hours and additional shift to complete a project. Complete assignments under minimal supervision; work well independently and as team ... - 2023 May 01