Google Cloud Platform SOP Writer (Contractor)

Overview

Remote
Depends on Experience
Contract - W2
Contract - Independent

Skills

Attention To Detail
Clarity
Collaboration
Operational Excellence
Management
SOP
GxP
WIS
Google Cloud Platform
Editing
Documentation
Pharmaceutical Industry
Regulatory Compliance
Good Clinical Practice
Innovation
Organizational Skills
Standard Operating Procedure
Writing
Startups
Inspection
Biotechnology

Job Details

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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.

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.

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