I will write sops for gmp, glp, iso 17025, quality systems
About this Gig
Need professional SOPs (Standard Operating Procedures) written according to GMP, GLP, or ISO 17025?
Im Özge Düzgün, a Chemical Engineer (M.Sc.) with over 6 years of experience in analytical laboratories and quality systems within the pharmaceutical, cosmetic, food supplement, and chemical industries.
Ive prepared and implemented SOPs for analytical methods, quality control, validation, documentation, and laboratory operations, ensuring compliance with international standards.
What I offer:
- Writing new SOPs for laboratory, production, or QA processes
- Revising or updating existing SOPs according to GMP, GLP, ISO 17025
- Creating SOP templates for recurring operations
- Including clear responsibilities, procedures, acceptance criteria, and documentation flow
- Aligning SOPs with ICH, WHO, and FDA standards
Deliverables:
- Editable Word document (professionally formatted SOP)
- PDF final version
- Revision history & document control section
Why choose me:
- Experience preparing hundreds of SOPs in regulated industries
- Scientific and regulatory accuracy
- Fast delivery & confidential project handling
Lets make your quality system stronger, compliant, and audit-ready!
Domain:
Consulting
Industry:
Business services & consulting
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Wellness
Language:
English
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Turkish
FAQ
Do you write SOPs for analytical methods?
Yes! I can prepare SOPs for HPLC, GC, UV-Vis, sample prep, documentation, validation, etc.
Will the SOPs meet GMP / GLP / ISO 17025 requirements?
Absolutely. All SOPs are written according to global standards and structured for audit readiness.
Can you adapt the SOPs to my company’s format?
Yes — you can send your template, and I’ll follow your format exactly.
