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QC Lab LEQ ValidationTechnical Writer I
Ref No.: 15-03717
Location: Framingham, Massachusetts
Duties:
Draft protocols and reports for Laboratory Equipment Qualification (IQ, OQ, and PQ) according to company policies.
Assist multiple teams of technical experts in the technical writing of Laboratory Equipment Qualification Requires working with Quality Control staff that will provide document redlines and review completed work.
Revisions of Laboratory Equipment Qualification documentation must be done utilizing defined content and formatting requirements.
The Technical Writer must be familiar with Microsoft Office products including Word, Excel, and PowerPoint.
Prior experience with Livelink a plus.
This person should be very familiar with documenting Laboratory Equipment Qualification / Validation studies, specifically pertaining to Quality Control.
Familiarity with cGMP is required.
Organize documentation and cross-reference documents as necessary.
Edit, standardize, or revise material prepared by other writers or subject matter experts.
Prepare rough drafts of the documentation for review with subject matter experts, project staff and/or customers.
Technical writer will be trained in company SOP documentation standards, templates and practices.
 
Skills:
Technical writer must write in a concise and easy-to-read manner.
The Technical Writer will create and revise Laboratory Equipment Qualification / Validation Protocols and Reports from input of subject matter experts.
Excellent writing and editing skills.
Able to actively listen to what other people are saying and ask questions as appropriate.
Able to work with new material or information to grasp its implications.
Able to type 50 - 60 words/min Proficient with MS Word, Excel, and PowerPoint
 
Education:
Bachelor's Degree required