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I will write pharmaceutical sops, method of analysis
About this Gig
Are you looking for a pharmaceutical professional to write or review your SOPs, Methods of Analysis, or QC Chromatograms? You're in the right place!
With over 10 years of experience in pharmaceutical quality control and documentation at Pharmaceutical Industry, I specialize in drafting and reviewing:
- Standard Operating Procedures (SOPs)
- Analytical Methods of Analysis
- HPLC/UPLC/GC Chromatogram Review
- Compliance with GMP, GLP, ALCOA+ Principles
- GAP Analysis and Data Integrity Checks
- Specifications and COA Alignment
- ISO 9001:2015 Audit Documentation
- Audit CAPA management
I ensure that all documents meet regulatory standards, follow best laboratory practices, and are aligned with ICH, USP, BP and GMP guidelines.
Whether you're a startup lab, a contract manufacturer, or a regulatory consultant. I'll provide precise, compliant, and audit-ready documentation tailored to your needs.
Why Choose Me?
- 10+ years in pharma QC (including HPLC, UPLC, FTIR, ICP-OES)
- Certified GMP Auditor & GLP Trained
- Skilled in Minitab & SAP ERP for pharma documentation
- Delivered 500+ pharma documents & protocols
- Responsive and detail-oriented
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Document type:
User & training manuals
•
Documentation
Industry:
Medical & biotech
Language:
Bengali
•
English
Delivery style preference
Please inform the freelancer of any preferences or concerns regarding the use of AI tools in the completion and/or delivery of your order.
FAQ
Q1: What information do I need to provide to get started?
Please share the product/process name, target regulatory standard (e.g., GMP, USP, ICH), and any existing templates or data. I can also work from scratch if needed.
Q2: Can you create SOPs from scratch or only review existing ones?
I can do both — write new SOPs, revise outdated ones, or review and suggest improvements based on compliance standards and best practices.
Q3: Do you follow any specific regulatory guidelines?
Yes. I follow GMP, GLP, ICH Q2, ALCOA+, USP, and WHO guidelines, ensuring your documents meet audit and regulatory expectations.
Q4: What formats do you deliver in?
I deliver in editable Microsoft Word or PDF format. You may request Excel templates if applicable (e.g., logbooks, data sheets).
Q5: Are you experienced with analytical instruments and chromatograms?
Absolutely. I’ve worked hands-on with HPLC, UPLC, GC, FTIR, UV-Vis, and more. I can interpret and correct chromatograms, especially for QC compliance and audits.
