Senior Technical Writer – Medical Device & FDA Docs

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

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.