Google Cloud Platform SOP Writer (Contractor)
NO H1Bs PLEASE SHARE ME SUITABLE RESUMES
Job Title: Google Cloud Platform SOP Writer (Contractor)
Location: Remote
Duration: Long Term
Job Description:
Our client, a cutting-edge clinical-stage biotechnology company, is looking for a Google Cloud Platform SOP Writer (Contractor) to support the development and refinement of Clinical Operations SOPs and related GxP documentation. This role is ideal for seasoned professionals with a strong background in regulatory writing and a solid understanding of global clinical compliance standards. The position offers flexibility and the opportunity to work remotely while contributing to high-priority documentation projects.
Responsibilities:
- Develop, revise, and maintain Standard Operating Procedures (SOPs), Work Instructions (WIs), and other GxP-related documentation.
- Collaborate closely with internal stakeholders to collect information, document processes, and ensure clarity in written procedures.
- Ensure all documentation aligns with Google Cloud Platform, ICH, and FDA/EMA regulatory expectations and is inspection-ready.
- Propose shared SOP frameworks and standardization opportunities across departments.
- Produce clear, concise, and easy-to-navigate documents to support operational excellence.
Qualifications:
- At least 8 years of experience in the biotech or pharmaceutical industry; experience in startup environments is a plus.
- Minimum 5 years of hands-on experience developing and editing GxP SOPs, with at least 3 years focused on Clinical Operations SOPs.
- In-depth knowledge of Google Cloud Platform, ICH guidelines, and global regulatory requirements (FDA/EMA).
- Strong writing, editing, and organizational skills with high attention to detail.
- Ability to manage multiple tasks and shifting priorities in a fast-paced setting.
- This is a remote-friendly role, requiring availability for 20 to 30 hours per week.
This contract opportunity provides the chance to make a meaningful impact on clinical documentation and regulatory compliance for a company at the forefront of biotech innovation.
NO H1Bs PLEASE SHARE ME SUITABLE RESUMES
Job Title: Google Cloud Platform SOP Writer (Contractor)
Location: Remote
Duration: Long Term
Job Description:
Our client, a cutting-edge clinical-stage biotechnology company, is looking for a Google Cloud Platform SOP Writer (Contractor) to support the development and refinement of Clinical Operations SOPs and related GxP documentation. This role is ideal for seasoned professionals with a strong background in regulatory writing and a solid understanding of global clinical compliance standards. The position offers flexibility and the opportunity to work remotely while contributing to high-priority documentation projects.
Responsibilities:
- Develop, revise, and maintain Standard Operating Procedures (SOPs), Work Instructions (WIs), and other GxP-related documentation.
- Collaborate closely with internal stakeholders to collect information, document processes, and ensure clarity in written procedures.
- Ensure all documentation aligns with Google Cloud Platform, ICH, and FDA/EMA regulatory expectations and is inspection-ready.
- Propose shared SOP frameworks and standardization opportunities across departments.
- Produce clear, concise, and easy-to-navigate documents to support operational excellence.
Qualifications:
- At least 8 years of experience in the biotech or pharmaceutical industry; experience in startup environments is a plus.
- Minimum 5 years of hands-on experience developing and editing GxP SOPs, with at least 3 years focused on Clinical Operations SOPs.
- In-depth knowledge of Google Cloud Platform, ICH guidelines, and global regulatory requirements (FDA/EMA).
- Strong writing, editing, and organizational skills with high attention to detail.
- Ability to manage multiple tasks and shifting priorities in a fast-paced setting.
- This is a remote-friendly role, requiring availability for 20 to 30 hours per week.
This contract opportunity provides the chance to make a meaningful impact on clinical documentation and regulatory compliance for a company at the forefront of biotech innovation.