Technical Writer
Artech Information System LLC, Andover, MA, United States
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.
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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.
#J-18808-Ljbffr