Artech Information System LLC
Technical Writer
Artech Information System LLC, Andover, Massachusetts, us, 05544
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
Job Description:
If you want to know about the requirements for this role, read on for all the relevant information.1) Excellent oral and written communications with experience in technical writing of reports and/or regulatory documents2) Regulatory, GMP or Pharmaceutical experience, preferably in bioprocess or cell line development areas is desirable3) Detail oriented
Job Responsibilities:
The BRD organization within the Pharm Sci BTx organization needs to hire a technical writer. This colleague will perform the following activities:(1) Assist with verification of data within regulatory documents or reports.(2) Support the bioprocess R&D (BRD) teams in tracking document completion, data verification strategies and completion of edits.(3) Create drafts of new technical or regulatory documents using existing examples, templates or reports.(4) Assist Bioprocess team authors in assembling, formatting, and proofreading figures, tables and content.(5) 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:
If you want to know about the requirements for this role, read on for all the relevant information.1) Excellent oral and written communications with experience in technical writing of reports and/or regulatory documents2) Regulatory, GMP or Pharmaceutical experience, preferably in bioprocess or cell line development areas is desirable3) Detail oriented
Job Responsibilities:
The BRD organization within the Pharm Sci BTx organization needs to hire a technical writer. This colleague will perform the following activities:(1) Assist with verification of data within regulatory documents or reports.(2) Support the bioprocess R&D (BRD) teams in tracking document completion, data verification strategies and completion of edits.(3) Create drafts of new technical or regulatory documents using existing examples, templates or reports.(4) Assist Bioprocess team authors in assembling, formatting, and proofreading figures, tables and content.(5) 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