Copy Editor

Responsibilities Design, prepare, and revise Electronic Batch Records (EBR). Support end users with EBR execution and usage. Manage EBR design/configuration changes, process reviews, and alignment with continuity-plan documentation. Initiate and own change controls for documents and equipment; ensure timely closure and implementation. Participate in process mapping; engage SMEs, leads, and operators to ensure critical parameters are captured. Serve as sustainment point of contact for electronic batch record manufacturing issues; Execute functional verification protocols for MES/recipe design and baseline configuration. Support continuous improvement and applicable batch record changes. Follow up on BT tickets and ensure resolution of EBR issues. Ensure activities comply with procedures; identify deviations/exceptions and escal Adhere to safety procedure and GMP/GDP practices. Reassess/participate in agile change environment to drive continuous improvement; support projects/deployments. Participate in cross-functional teams to support, enhance, and upgrade AMPS. Assist with controlling/tracking periodic EBR procedure updates and manage emergency changes. Attend scheduled training and provide cross-training across AMPs areas. Qualifications/Requirements Bachelor’s (0+ years) OR Associate’s (4 years) OR High school diploma (6 years) in relevant field. Pharmaceutical experience. Certifications: M1, Yellow Belt and/or Pfizer Human Performance methodology. Computer skills: HTML, Java, or object-oriented programming. Focused in systems analyst/data management. EBR/MES build experience. Experience working in Quality Tracking Systems. Application Authorize to work in the U.S. (visa sponsorship not available for this role). #J-18808-Ljbffr