2

Remote Policy Procedure Writer Jobs in California

San Diego, USA- Remote Be a part of a global team that is inspired to make a difference in the ... procedures through innovation and adoption of industry best practices and drive alignment across ...

Legal Writing & Editing * Court Filings & Case Material Review * Legal Research & Summarization ... Licensed to practice law with demonstrated expertise in criminal law and procedure. * Significant ...

Legal Writing & Editing * Court Filings & Case Material Review * Legal Research & Summarization ... Licensed to practice law with demonstrated expertise in criminal law and procedure. * Significant ...

Legal Writing & Editing * Court Filings & Case Material Review * Legal Research & Summarization ... Licensed to practice law with demonstrated expertise in criminal law and procedure. * Significant ...

Showing results 21-40

Remote Policy Procedure Writer information

What is the difference between Remote Policy Procedure Writer vs Remote Compliance Analyst?

AspectRemote Policy Procedure WriterRemote Compliance Analyst
CredentialsWriting certifications, industry-specific knowledgeCompliance certifications (e.g., CPA, CCEP), analytical skills
Work EnvironmentPrimarily writing, editing, policy developmentMonitoring, auditing, regulatory analysis
Industry UsageLegal, HR, corporate policy sectorsFinancial, healthcare, regulatory sectors
Search/Comparison IntentUnderstanding writing roles in policiesUnderstanding compliance and regulatory roles

While both roles involve understanding industry standards, the Remote Policy Procedure Writer focuses on creating and updating policies, whereas the Remote Compliance Analyst concentrates on ensuring adherence to regulations. Both roles require industry-specific knowledge but serve different functions within organizations.

What job categories do people searching Remote Policy Procedure Writer jobs in California look for?

The top searched job categories for Remote Policy Procedure Writer jobs in California are:

What cities in California are hiring for Remote Policy Procedure Writer jobs?

Cities in California with the most Remote Policy Procedure Writer job openings:

Infographic showing various Remote Policy Procedure Writer job openings in California as of August 2026, with employment types broken down into 85% Full Time, and 15% Part Time. Highlights an 5% In-person, and 95% Remote job distribution.

Technical Writer - Product Development (Dental Devices)

Prismatik

Irvine, CA • On-site, Remote

$30 - $43/hr

Full-time

Re-posted 9 days ago


Job description

We're looking for a Technical Writer to help turn complex technical and scientific information into clear, well-structured documentation. From SOPs and test methods to IFUs and technical reports, you'll play a key role in making sure our products are accurately documented and ready for market.
Essential Functions:
  • Collaborates with Research & Development, Manufacturing and Marketing teams to accurately document test methods, technical reports, labels, and other design file documents for specific market products.
  • Performs independent literature research, analyzes data and conducts interviews for in-depth white papers and other scientific/technical documents.
  • Conducts extensive literature and industry research, analyzes results and compiles information into meaningful reports for various audience types.
  • Performs interviews with scientific and technical staff, and translates information onto detailed documents.
  • Creates all essential documentation for technical device design histories, manufacturing BOMs and routers.
  • Works closely with regulatory and quality staff to ensure product documentation supports regulatory and quality standards.
  • Works with project and product managers to document product alignment with business strategy.
  • Designs and creates protocols, technical reports, test methods, manufacturing instructions, project planning documents and labeling documents.
  • Designs marketing documents, IFUs and labels according to the Quality System.
  • Supports project managers with action items, project planning documentation, and coordinates with the project team for successful launch of product.
  • Creates Standard Operating Procedures (SOPs) for new procedures; maintains and updates current SOPs.
  • Creates technical submission files and coordinates with regulatory team on submission/approval process.
  • Collaborates with regulatory team to assist with international submissions; creates additional required documents as new regulations arise in different countries.
  • Coordinates, validates, and assists with documenting test results.
  • Performs other related duties and projects as business needs require at direction of management.
Minimum Qualifications:
  • Bachelor's Degree in Engineering, Science or a related technical field.
  • Minimum of four (4) years of direct documentation experience in the medical device, software or other technical industry.
  • Knowledge of 21 CFR 820.
  • Knowledge of current US and International regulations as it pertains to documentation.
  • Knowledge of current US and International standards governing medical devices.
Pay range: $30.00 to $43.00/hr
Exact compensation may vary based on skills and experience.
This role is fully onsite at our Irvine, CA campus. Remote or hybrid arrangements are not available.
Employment Type: full-time