Pharmaceutical QC Technical Writer - Contractor

EY - Newark, NJ - Contract Description We currently have a contract opportunity for a Pharmaceutical QC Technical Writer Assist in the technical writing of the project team as guided by the company's PM and/or in conjunction with the SOPs defined on the company's SDLC website Help teams execute with the company's SDLC framework and in consideration with the GXP compliance criteria of this solution Gather, document, and/or edit required SDLC documents as required by the company's SDLC SOPs unless otherwise noted by Quality Project Team members Write and review test cases, test scripts, test scenarios, and test results to verify the segregation rules and data migrations are in place and functioning as required Liaison with the company's stakeholders as needed to align on the company's best practices and policies on data segregation, validation Contract duration is 6 - 12 months. Skills quality control technical wri... Qualifications Significant experience in working projects structured a... - Contract - Full-time

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