May be responsible for coordinating the display of graphics and the production of the document.
Writes a variety of technical articles, reports, brochures, and/or manuals for documentation for a wide range of uses.
Paper batch record authoring/revision/template creation
CAPA execution/follow-up for doc revisions
SOP revisions/authoring
Update/create training documents w/ training specialist.
Familiar with a variety of the fields concepts, practices, and procedures.
Strong technical writing skills
Experience authoring and revising cGMP documentation for commercial operations.
Advanced proficiency in MS Word
Working knowledge of cGMP document control systems
Intermediate knowledge of biopharmaceutical operations preferred
Bachelors Degree
Technical writing certification preferred.
> 2 years relevant experience in the pharmaceutical, biotech, medical device, or other regulated environment