Viewing 11 - 20 of 40 jobs
Design, Process Risk Assessment, Technology Transfer Plan, Validation Master Plan, etc. * Ensure that all technology ... / Senior Principal Pharmaceutical Scientist or Engineer: * Requires an advanced degree in a...
processes and related systems, techniques used in validation and applicable CGMP regulations. - Provides ... BS Engineering Skills:- 10 years experience in validation/GMP- 3 years project lead experienceJoul offers...
validation activities. The Commissioning and Qualification Engineer will also provide support for Company process and ... with a variety of departments such as Validation, Engineering, Project Management and Quality...
Summary The Phased Array and Signal Processing Quality Engineer is responsible for developing test suite or test ... tests Report bugs and verifying fixes Perform final product validation Required Qualifications A bachelor's degree and 3...
CHEMICAL ENGINEER: Technical Services / Protein Purification SUMMARY: We are looking for a highly motivated and self-dir ... of large scale column packing, process chromatography validation, and process chromatography method development *...
Meta provides the unique core capabilities of data validation, integration, and resulting integrity upon which all subsequent data activities rely namely, information reporting, analysis, and program management. Solutions are designed to...
and network-level controllers as required. Assists in validation of complete system functionality and troubleshoots problems with project team to ensure proper operation. Designs and configures hardware and software for control system...
interface for model-based design, simulation, verification, validation, and testing applications. The ideal candidate for this roleis familiarwithhandling large data sets, experienced working within a large code base, and interested in...
documentation, process and hardware verification/validation 3) Oversee supplier quality and systemic improvements to the quality management system 4) Review/approval of supplier data associated with product and specification changes 5)...
analytical methods, including author and execute method validation protocols and write final reports. - Develop and review quality documents including SOPs, QIPs, RIPs, and TOPs. - Serve as an SME for laboratory analytical method...