Technical Writer

• Writing methods, protocols, reports, SOPs and evaluating compendia procedures as it impacts the pharmaceutical products or raw materials.
• Responsible for supporting the scientists in R&D to prepare the documentation as required by clients, including follow up of change controls, maintaining the templates for laboratory documents.
• Responsible for periodic review of the compendia changes and providing evaluation as it impacts the Raw Material, Finished Product and R&D groups within Analytical Operations.
• Write or review protocols for method development, feasibility, transfer, verification, and validation projects in collaboration with R&D personnel.
• Write or review client methods for routine sample analysis as needed.
• Collect and provide the necessary documentation for R&D projects, such as sample specifications, method details, and validation reports.
• Ensure the testing instructions are timely available and unambiguous, to facilitate the bench work complete as scheduled.
• Document analytical findings by compiling data into standardized report templates.
• Review the compendia updates (e.g., USP, EP, JP), document changes, and communicate updates to relevant departments.
• Act as a technical resource for team members, providing guidance on documentation issues.
• Track the progress of R&D projects to ensure completion, including document organization.
• Inform the appropriate manager if assigned work cannot be completed within the expected timeframe and quality standards.
• 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.

Technical Writer II – H&N Pharma, R&D

Senior Technical Writer

Technical Writer, Automotive Industry