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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
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
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
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
Moorestown, NJ
... CRM, CSV, Data Integrity, Disaster Recovery, Docspace, Documentum, Dynamics 365, EDMS, Excel, FirstDoc, FrameMaker, Front Page, GMP, GCP, GLP, HP ALM, HTML, IaaS, Interviewing, ISO, ITIL, IQ / OQ / PQ, Jenkins, Jira, LIMS, LMS, Maximo, Metadata, MS ...
- 2023 May 24
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
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
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
Monmouth Junction, NJ
... against priorities according to business importance and impact Lead the overall execution of multiple technical projects regarding initiation, budgeting, scheduling, monitoring, and closure according to GMP, safety and environmental requirements. ...
- 2023 Apr 15
Feasterville, PA
... Responsible for maintaining GxP (GCP, GLP and GMP) compliance. Implemented Electronic Document Management system and Learning Management System (Veeva) Knowledge of drug development process, US FDA Regulations, IND, NOA, ICH (Including Good Clinical ...
- 2023 Apr 10