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The Technical Writer is responsible for the creation of batch records for use in GMP manufacturing of new custom products. This technically sound position works cross functionally at multiple manufacturing facilities with Manufacturing, Process and Analytical Development, Quality, Project Management, and customers to develop robust manufacturing batch records from Tech Transfer documents. We're looking for a candidate with strong composition skills and comprehensive technical knowledge and understanding of manufacturing equipment and production processes. The position will be based in St. Louis, Missouri. Who You Are Minimum Qualifications: Bachelor's degree in Biology, Chemistry, Biochemistry or another life science discipline.2 + years' experience in GMP Operations, manufacturing or production operations. Preferred Qualifications: 5 + years' experience in GMP Operations, manufacturing or production operations.1+ years' experience writing GMP batch records.Excellent attention to detail in written instruction and communication.Strong composition skills - Able to convey technical, safety, and GMP compliance information and instruction through writing.Comprehensive technical knowledge and understanding of GMP manufacturing equipment and production processes.Ability to effectively communicate with internal departments and customers.RSREMD