Kategorien durchsuchen
Entdecken
Fiverr Pro
Deutsch
$
USD
I will proofread and edit gmp sops, QA documents, and gmp compliance texts
GMP Compliance und QA Expertise
I am a licensed pharmacist with over 3 years of experience in the pharmaceutical industry. In my role as a (Senior) QA Specialist for GMP Compliance, with a focus on CSV, data integrity, and qualifica...
Über diesen Service
As a Senior QA Specialist for GMP compliance with 3+ years of experience in the German pharmaceutical industry, I offer professional proofreading and editing for GMP documents aligned with EU-GMP and ICH standards.
I revise SOPs, QA documents, risk assessments, user requirement specifications, validation plans, and qualification protocols (VP and QP including IQ, OQ, PQ plans) ensuring clarity, regulatory consistency, and audit readiness.
You will recieve:
- Structural edits and compliance checks
- fact checking
- feedback for improvement
- document delivery in word or pdf in english or german language
Packages scale from single documents (Basic) to full project sets (Premium, up to 10,000 words).
Optional add-ons include fast delivery and extra revisions.
My Premium package is designed for full project reviews, covering one document of each type (e.g., VP, URS, Risk, SOP). The 10,000-word limit reflects typical GMP verbosity not strict content density. Prior discussion is welcome to clarify what counts toward the word total and whats excluded (e.g., headers, tables, annexes), so you get a truly premium experience.
Sprache:
Englisch
•
Deutsch
Content-Typ:
Technische Dokumentation
•
Dokumente
•
Andere
Bevorzugte Lieferart
Bitte informiere den Freelancer über alle Präferenzen oder Bedenken in Bezug auf den Einsatz von KI-Tools bei der Ausführung und/oder Lieferung deines Auftrags.
FAQ
What types of GMP documents do you proofread and edit?
I specialize in SOPs, QA documents, risk assessments, validation plans (VP), and qualification protocols (CP) including all phases of validation/qualification (e.g. IQ, OQ, PQ), all aligned with EU-GMP and ICH guidelines. I do not usually work with FDA or USP regulated content.
What does the Premium package include?
The Premium package is designed for full GMP documentation sets. It typically covers one document of each type (e.g., VP, QP, Risk Assessment, SOP, URS), with a total word count of up to 10,000 words. This shall allow for a complete project review without being restricted by document type.
How is the word count calculated for Premium?
The 10,000-word limit reflects typical GMP verbosity. I focus on meaningful content — headers, annexes, tables, and boilerplate sections as well as repetitive parts may be excluded from the count. I encourage prior discussion to clarify what will be included so you get a fair and transparent review.
Can I request documents in both English and German?
Yes. I offer delivery in either English or German. If you need both versions, I can provide dual-language delivery as an optional add-on.
Do you offer fast delivery for urgent projects?
Yes. Fast delivery is available for all packages, including Premium. This is ideal for audit preparation, CAPA deadlines, or validation timelines. Please select the appropriate add-on when ordering.
Do you check for plagiarism or AI-generated content?
I do not check documents for plagiarism or AI-generated content.
Can I send multiple documents for review?
Yes. For Standard and Premium packages, you can submit multiple connected documents. I’ll treat them as a unified set and ensure consistency across all files.
