I will write or review sops or other gmp documents

United States

I speak English, Japanese

3 orders completed

Process Validation Engineer in Pharmaceuticals

Validation and process engineer with 8 years of experience in GMP-regulated pharmaceutical and biotech environments. I specialize in drafting and reviewing SOPs, validation protocols (IQ/OQ/PQ), batch...
About this Gig

I am a validation and process engineer with 8 years of experience in GMP-regulated pharmaceutical and biotech environments. I help companies create clear, compliant, and practical documentation needed for regulatory readiness and smooth operations.

I can assist with:

  • SOP drafting and revision
  • Validation protocols (IQ, OQ, PQ, PV, CV)
  • Batch record and logbook templates
  • Change control and deviation documentation
  • Documentation review and proofreading

Whether you are a startup building your quality system or an established team needing extra support, I deliver professional, audit-ready documents tailored to your process.

All work is confidential, well-organized, and delivered on time.

Document type:

Documentation

Reports

Language:

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.