Technical Writer

Artech Information System LLC; Andover (MA); On-site; Full time

Job summary

A leading IT staffing company is seeking a detail-oriented individual to assist with regulatory documents and reports. The ideal candidate will have excellent communication skills and experience in technical writing, particularly in the pharmaceutical or bioprocess areas. You will support R&D teams, create regulatory drafts, and utilize document management systems. This position is primarily based in Andover, MA, with flexibility for Chesterfield, MO as a secondary location.

Qualifications

• Experience in technical writing of reports and regulatory documents.
• Regulatory, GMP or Pharmaceutical experience in bioprocess or cell line development is desirable.

Responsibilities

• Assist with verification of data within regulatory documents or reports.
• Support the bioprocess R&D teams in tracking document completion and data verification strategies.
• Create drafts of new technical or regulatory documents using templates or reports.
• Assist Bioprocess team authors in assembling and proofreading figures and tables.
• Prepare documents using Regulatory templates in Microsoft Word.

Skills

Excellent oral and written communication

Detail oriented

Tools

Microsoft Word

GDMS document management system

Job description

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill‑sets availability, deliver emerging technology skill‑sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.

Job Description

• Excellent oral and written communications with experience in technical writing of reports and/or regulatory documents
• Regulatory, GMP or Pharmaceutical experience, preferably in bioprocess or cell line development areas is desirable
• Detail oriented

Job Responsibilities

• Assist with verification of data within regulatory documents or reports.
• Support the bioprocess R&D (BRD) teams in tracking document completion, data verification strategies and completion of edits.
• Create drafts of new technical or regulatory documents using existing examples, templates or reports.
• Assist Bioprocess team authors in assembling, formatting, and proofreading figures, tables and content.
• Prepare documents using Regulatory templates in Microsoft Word and Predict and work within GDMS document management system.

Scope of Work

This position is preferred to be located in Andover, MA; however, the Chesterfield, MO site would also be an acceptable location.