Technical Writer II (Pharma)
Core
Compile accurate scientific reports and verify data consistency from analytical instruments in a pharma setting.
Role type
Scientific data analyst and documentation specialist
Builds
Validated scientific reports, test outputs, and regulatory documentation
Domain
Pharmaceutical industry, analytical chemistry, quality assurance
Required skills
Scientific data entry, report creation, analytical method understanding, regulatory compliance (cGMP/GcLP), SOP management, spreadsheet validation
Preferred skills
Knowledge of ICH M10, pharmacopeias (EP, USP), software re-validation scripting
Technologies
Microsoft Office Suite (Word, Excel, PowerPoint, Outlook), analytical instruments
Responsibilities
Compile scientific reports using validated data from analytical instruments, crosscheck data consistency across techniques, execute predefined test scripts for software re-validation, review and approve department SOPs and testing worksheets, document analytical findings in standardized templates, communicate compendia updates to relevant departments (via careerplan.io/jobs/744000153404749-technical-writer-ii-pharma-at-sgs)
Seniority
Mid-level, hands-on IC
