Deviation Writer Intellectt INCDeviation WriterIndianapolis, INThis role partners with Manufacturing, Engineering, MS&T, Supply Chain, and Quality teams to develop clear, data-driven deviation investigations, identify root causes, and implement effective CAPAs. We are seeking an experienced Deviation Writer to support investigation writing and root cause analysis within a GMP-regulated manufacturing environment.
Technical Writer GxP & Validation Documentation inSync StaffingTechnical Writer GxP & Validation DocumentationIndianapolis, INJOB SUMMARY: Theoris is looking for someone who will author and maintain validation-ready documentation while working closely with engineers, product managers, and subject matter experts to translate complex technical systems into clear, auditable content. Translate complex system configurations, API behaviors, Veeva Vault Safety workflows, and integration logic into GxP-compliant documentation.
Deviation Writer INCOG BioPharma Services IncDeviation WriterFishers, INThe Deviation Writer will work closely with the Manufacturing, Production Engineering, Manufacturing Sciences and Technology, Supply Chain, Quality, and other cross-functional teams to create comprehensive investigations that leverage facts and data to support robust root cause conclusions, effective corrective actions, and systematic all-encompassing preventative actions. The Deviation Writer will exemplify excellent interpersonal skills and be capable of developing productive customer-centric working relationships with internal and external customers and have a role with high visibility to all departments.
Technical Writer- LabVantage StratAcuity Staffing Partners IncTechnical Writer- LabVantageIndianapolis, INRemote$40–$55 / hourIn terms of professional development, Everforth Apex hosts an on-demand training program, provides access to certification prep and a library of technical and leadership courses/books/seminars once you have 6+ months of tenure, and certification discounts and other perks to associations that include CompTIA and IIBA. Technical Writer supports a global LabVantage LIMS implementation by authoring, revising, and managing GMP documentation including SOPs, forms, job aids, and validation evidence.
Specification Writer INCOG BioPharma Services IncSpecification WriterFishers, INWork closely with Supply Chain, vendors, Quality, project teams, and clients to gather necessary technical information, facilitate effective communication, and ensure that all documentation reflects the latest material information and stakeholder feedback. If you crave the challenge of creating systems from scratch and believe you have insights for a better way of doing business, which benefits customers by ensuring quality outcomes and accelerating their route to market, we want to hear from you.