The BioPharma Technical Writer is responsible for developing, reviewing, and maintaining controlled documentation that supports validation and laboratory operation activities. This role ensures that standard operating procedures (SOPs), forms, protocols, and other technical documents are accurate, clear, and compliant. The Technical Writer collaborates with cross-functional subject matter experts to manage documents, support quality initiatives, and promote consistency and continuous improvement.Technical Writer Duties Include but are not Limited to the Following:BioPharma Technical Writer IWrite and edit forms, protocols, reports, and procedures from existing templates under supervision.Analyze documents to maintain continuity of style and content.Perform updates and revisions to technical documents as instructed.Work with Scientists, Regulatory Affairs, and Research and Development in a collaborative manner.Other duties as assignedBioPharma Technical Writer IIAs above, plus:Mentor/train new associates.Write documents from templates with minimal assistance.Create/modify document templates as needed.Participate in additional training (specific technical/scientific writing, regulatory affairs, clinical trials, statistics specific scientific topics, etc.).Participate in additional projects such as process improvement initiatives, presenting at a departmental meeting, etc.Other duties as assigned