I’m a documentation and quality professional with over [8 years] of experience in pharmaceutical and ISO 17025:2017 laboratory systems.
Developing and reviewing ISO 17025 documentation (SOPs, QA/QC manuals, calibration records, etc.)
Data cleaning, entry, and organization in Excel and CRMs
File conversion, formatting, and professional report writing
I ensure accuracy, compliance, and clarity in every project.
✅ 100% Verified Profile
✅ Fast and Clear Communication
✅ Committed to Quality & On-time Delivery
Work Terms
I provide accurate, well-formatted, and standard-compliant documentation for ISO/IEC 17025:2017 and PNAC requirements.
All work is delivered on time with clear communication throughout the project.
I prefer milestone-based or hourly payments through Guru SafePay for mutual security.
Revisions are free within the agreed project scope to ensure client satisfaction.
Documents are shared in MS Word and PDF formats, properly formatted and ready for use.
I maintain confidentiality of all client data and laboratory information.
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