Technical Writer

Job Description:
1) Excellent oral and written communications with experience in technical writing of reports and/or regulatory documents
2) Regulatory, GMP or Pharmaceutical experience, preferrably in bioprocess or cell line development areas is desirable
3) 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.
This position is preferred to be located in Andover, MA; however, the Chesterfield, MO site would also be an acceptable location.

Regards,

Anuj Mehta

973-967-3402