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Skills
Document Controlunmatched
Documentationunmatched
Manufacturing Requirementsunmatched
Medical Equipmentunmatched
Process Improvementunmatched
Product Documentationunmatched
Proofreadingunmatched
Regulatory Requirementsunmatched
Source Code/Configuration Management (SCM)unmatched
Support Documentationunmatched
Technical Editingunmatched
Technical Writingunmatched
Description
Responsibilities:
- Create, edit, and maintain technical documents, manuals, work instructions, and procedures.
- Review and update documentation to reflect product and process changes.
- Collaborate with Engineering, Quality, Regulatory, and Manufacturing teams.
- Organize technical information into clear, user-friendly documentation.
- Ensure documents comply with company standards and regulatory requirements.
- Support document control, version management, and revision activities.
- Proofread documents for grammar, formatting, consistency, and technical accuracy.
- Prepare patient-facing and medical device documentation when required.
- Maintain accurate documentation and support continuous process improvements.
Numbers & Facts
| Location | Los Angeles, CA |
| Job Type | Contractor |
| Salary | $20–$22 Per Hour |
Qualifications
Required Qualifications:
- Bachelor's degree required.
- Experience writing technical or patient-facing documentation.
- Strong written and verbal communication skills.
- Excellent attention to detail and organizational skills.
- Proficiency in Microsoft Word, Excel, Outlook, and PowerPoint.
Preferred Qualifications:
- Experience in the medical device or regulated industry.
- Knowledge of document control and quality management systems.
- Ability to work independently and collaborate with cross-functional teams.
- Strong editing, proofreading, and technical writing skills.