Technical Writer II (Pharma)

Primary Responsibilities
• As a member of the team in our Global Business Solutions (GBS) center, the Technical Writer (Level I) will be responsible for compiling accurate scientific reports using validated data from analytical instruments. Verify data consistency across techniques, identify and report discrepancies.
• Additionally, execute predefined test script for regular software re-validation, and report test outputs.
• Assist in the revision, creation, review and approval process for appropriate department SOPs, testing worksheets, and forms.

Specific Responsibilities
• Compile scientific reports using validated data from various analytical instruments. Produce clear, structured, high‑quality documentation following scientific conventions and internal templates.
• Crosscheck and verify data consistency across different analytical techniques to ensure results logically correspond before report finalization. Report on anomalies in the outputs.
• Execute predefined test scripts as part of scheduled software revalidation activities, accurately documenting and reporting all resulting outputs. Identify and report discrepancies observed during testing. Perform retesting once updates have been applied.
• Document analytical findings by compiling data into standardized report templates.
• Review the compendia updates (e.g., EP, USP), document changes, and communicate updates to relevant departments.
• Assists with writing and reviewing testing worksheets, protocols and reports. Ensure approval for department SOPs, worksheets, and forms. Perform spreadsheet validations according to SOP.
• Performs other related duties as may be assigned either in support of departmental goals or for his/her personal or professional training, education or development as programmed by his/her immediate superior.
• At all times, comply with SGS Code of Integrity and Professional Conduct and with all SGS QHSE and HR policies and procedures. Ensure the work area in GBS is always clean and presentable.