Browse categories
Explore
Fiverr Pro
English
$
USD
I will write gmp and iso 17025 compliant lab sops for pharma, food and industrial labs
Lab SOP and QC Documentation Specialist for Industrial and Clinical Labs
I help laboratories and healthcare companies create ISO, GMP, and GLP compliant SOPs and QC documentation. As a Biomedical Engineer with hands-on experience in medical and analytical equipment, I deli...
About this Gig
Is your lab or company due for an audit and your SOPs are missing, outdated or not compliant?
I help pharmaceutical, food, FMCG, medical device and clinical laboratory companies create professional, audit-ready SOPs and QC documentation that meet ISO 9001, GMP, GLP, ISO 17025 and ISO 13485 requirements delivered remotely and fast.
As a Biomedical and Analytical Instrumentation Engineer with hands-on field experience across regulated industries, I don't just write documents I write SOPs that actually reflect how your processes work, structured the way auditors expect to see them. Every document I deliver is standardised, regulation-aligned and built to pass not just to exist.
What I cover: SOPs for analytical equipment (HPLC, balances, pH meters, incubators and more), QC and testing reports, lab manuals, equipment logbooks, audit checklists, calibration procedures and full compliance documentation.
What every document includes: Purpose, Scope, Responsibilities and step-by-step Procedure properly structured, version controlled, with signatory approval blocks and revision history. All work is aligned with ISO 9001, ISO/IEC 17025, GMP, WHO and ALCOA+ data integrity principles.
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.
My Portfolio
FAQ
What type of laboratories do you work with?
I work with industrial, pharmaceutical, FMCG, oil & gas, manufacturing, and healthcare/clinical laboratories. My documentation is adapted to each lab’s regulatory and operational needs.
Are your SOPs compliant with ISO and GMP standards?
Yes. All documents are structured to align with ISO 9001, ISO/IEC 17025, GMP, WHO guidelines, and ALCOA+ data integrity principles where applicable.
Can you customize documents to our specific equipment or workflow?
Absolutely. I customize SOPs and QC documents based on your equipment type, lab processes, and regulatory environment. You can also request brand-specific or method-specific documentation.
Do you provide editable files?
Yes. Final documents are delivered in editable Word format, with optional PDF copies upon request.
Can you help prepare documents for audits or inspections?
Yes. I provide audit-ready SOPs, checklists, and documentation reviews to support internal audits, regulatory inspections, and quality assessments.
