Senior Technical Writer for Regulated Medical Devices

Indotronix Avani Group; San Diego (CA); On-site; USD 62,508 - 89,027; Full time

Job summary

A medical equipment manufacturer in San Diego is seeking a mid-senior level contractor for writing and editing. The role involves creating and maintaining technical documentation to meet regulatory requirements, focusing on user manuals and guides. Qualified candidates should have at least five years of experience in a regulated industry like pharmaceuticals or medical devices, along with proficiency in authoring tools like MadCap Flare and Adobe FrameMaker. The role is contract-based for 12 months with a pay range of $55.00/hr.

Qualifications

• Experience in a regulated industry such as medical devices or pharmaceuticals.
• Extensive experience with regulatory compliance processes.
• Highly collaborative with marketing, clinical, quality, and regulatory reviewers.
• Experience with authoring tools (MadCap Flare, Adobe FrameMaker, InDesign, Illustrator).
• Ability to manage the delivery of prioritized tasks.
• Ability to work independently and solve problems.
• Familiarity with electro-mechanical concepts.

Responsibilities

• Create and maintain technical documentation for regulatory submissions.
• Ensure documentation meets regulatory requirements and industry standards.
• Provide recommendations to optimize engineering data.

Job description

A medical equipment manufacturer in San Diego is seeking a mid-senior level contractor for writing and editing. The role involves creating and maintaining technical documentation to meet regulatory requirements, focusing on user manuals and guides. Qualified candidates should have at least five years of experience in a regulated industry like pharmaceuticals or medical devices, along with proficiency in authoring tools like MadCap Flare and Adobe FrameMaker. The role is contract-based for 12 months with a pay range of $55.00/hr.