Quality & Compliance Document Review and Rewrite
Budget / Salary$30–250
TypeFreelance project
LocationRemote
Posted1 hour ago
Hi! I’m looking for help with two related quality/compliance projects. I’d like someone to review the existing documents and help me develop polished, professional drafts that I can review internally.
**1. Internal Audit Program**
I need a comprehensive review of our current internal audit process across multiple sites. The goal is to determine how we can make the process more consistent and standardized across the business globally.
The work would include:
* Reviewing the current internal audit SOP(s), procedures, forms, templates, and related documents.
* Identifying gaps, inconsistencies, or areas that could be improved.
* Developing recommendations for how the internal audit process should work consistently across all sites.
* Updating or rewriting the applicable SOP(s) to reflect the improved/global process.
* Updating or creating the associated forms, templates, and supporting documentation as needed.
* Ensuring the documents work together as one cohesive, global internal audit process.
**2. Quality Manual / Quality Process**
I also have an existing quality process document/Quality Manual that was shared internally through SharePoint. I would like this document reviewed and, where necessary, substantially revised or rewritten.
The goal is to take the existing document and turn it into a clear, professional, globally applicable quality process. This would include:
* Reviewing the current Quality Manual/process.
* Identifying outdated, unclear, incomplete, or inconsistent sections.
* Rewriting sections where needed rather than simply making minor edits.
* Ensuring the process is structured logically and is appropriate for use across multiple sites.
* Reviewing any related SOPs, forms, or supporting documents and updating them as needed so everything is aligned.
* Producing a polished draft that is ready for internal review and approval.
**Overall Goal**
I’m looking for someone who can take the existing documentation, understand the intent and requirements, identify what needs to be improved, and turn it into a cohesive, professional, globally applicable set of quality documents. I would like the work to be developed to a point where it is close to completion and only requires my internal review and final adjustments.
Experience with **Quality Management Systems (QMS), internal audits, SOP development, regulated industries, GMP/GxP, pharmaceutical/biotech, or other highly regulated environments** would be strongly preferred.
**1. Internal Audit Program**
I need a comprehensive review of our current internal audit process across multiple sites. The goal is to determine how we can make the process more consistent and standardized across the business globally.
The work would include:
* Reviewing the current internal audit SOP(s), procedures, forms, templates, and related documents.
* Identifying gaps, inconsistencies, or areas that could be improved.
* Developing recommendations for how the internal audit process should work consistently across all sites.
* Updating or rewriting the applicable SOP(s) to reflect the improved/global process.
* Updating or creating the associated forms, templates, and supporting documentation as needed.
* Ensuring the documents work together as one cohesive, global internal audit process.
**2. Quality Manual / Quality Process**
I also have an existing quality process document/Quality Manual that was shared internally through SharePoint. I would like this document reviewed and, where necessary, substantially revised or rewritten.
The goal is to take the existing document and turn it into a clear, professional, globally applicable quality process. This would include:
* Reviewing the current Quality Manual/process.
* Identifying outdated, unclear, incomplete, or inconsistent sections.
* Rewriting sections where needed rather than simply making minor edits.
* Ensuring the process is structured logically and is appropriate for use across multiple sites.
* Reviewing any related SOPs, forms, or supporting documents and updating them as needed so everything is aligned.
* Producing a polished draft that is ready for internal review and approval.
**Overall Goal**
I’m looking for someone who can take the existing documentation, understand the intent and requirements, identify what needs to be improved, and turn it into a cohesive, professional, globally applicable set of quality documents. I would like the work to be developed to a point where it is close to completion and only requires my internal review and final adjustments.
Experience with **Quality Management Systems (QMS), internal audits, SOP development, regulated industries, GMP/GxP, pharmaceutical/biotech, or other highly regulated environments** would be strongly preferred.
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