Technical Writer-29088

OLSA Resources, Inc.; Princeton (NJ); On-site; USD 70,000 - 90,000; Full time

Job summary

A technical writing firm in Princeton seeks a Senior Technical Writer to reformat Risk Management Plan (RMP) documentation crucial for product definition. The ideal candidate will possess experience in the medical device industry, particularly in writing standard operating procedures (SOPs). Proficiency in Microsoft Word and Excel is essential. This role demands creativity and attention to detail, as well as familiarity with FDA regulations. Competitive compensation and a collaborative work environment are offered.

Qualifications

• Experience with FDA and regulated industry practices is preferred.
• Experience in writing SOPs and document changes is required.

Responsibilities

• Reformat Risk Management Plan (RMP) documentation.
• Update definitions and references in existing RMP documents.

Skills

Proficient in Microsoft Word: advanced editing, commenting, routing, formatting

Proficient in Microsoft Excel: editing, formatting

Technical Writing experience in the medical device industry

Education

Bachelor's degree or 4-6 years experience

Job description

Overview

This position is NonExempt. Hours over 40 will be paid at Time and a Half. Writes a variety of technical articles, reports, brochures, and/or manuals for documentation for a wide range of uses. May be responsible for coordinating the display of graphics and the production of the document. Familiar with variety of the field's concepts, practices and procedures. Relies on experience and judgment to plan and accomplish goals. May lead and direct the work of others. A wide degree of creativity and latitude is expected. May require a bachelor's degree or 4-6 years experience.

Notes from Manager

Technical writer to reformat our Risk Management Plan (RMP) documentation. Existing RMP documents are a critical part of the company's product definition. These documents need to be reformatted to include updated definitions and references. The senior technical writer should preferably have experience working with FDA - or other regulated industry – practices and ISO systems.

Qualifications

• Proficient in Microsoft Word: advanced editing, commenting, routing, formatting
• Proficient in Microsoft Excel: editing, formatting
• Prior experience Technical Writing in the medical device industry needed with particular emphasis in writing SOPs and document changes.