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DATE ADDED: Mon 18/05/2020

Technical Writer

South Lancaster, Massachusetts, US


JOB TYPE: Permanent, FullTime

Job Title: Technical Writer/Document Specialist (Must have Pharmaceutical domain experience) Location: Rensselaer, NY Type of Assignment: Full time Summary: Write , create, draft, edit, review and maintain documents designed to explain and test laboratory systems. Essential Duties and Responsibilities include, but are not limited to, the following: Creates and maintains technical writing standards. Writes, modifies/changes controlled documents. Writes, reviews, and maintains department standard operating procedures. Edit, standardize, or make changes to materials prepared by other writers or personnel. Coordinates projects and documentation assignments. Basic Qualification: BS/BA degree required 5 years of experience with bio pharmaceutical equipment or manufacturing, particularly in Quality Review required Preferred Qualification: Experience with: Good documentation practices (GDP) FDA regulated environments Laboratory systems Nonconformance and deviation management Building consensus among subject matter experts Process mapping Harmonizing documentation across groups Document control including document management systems LI-PS1