Job Description :
Pay Range $40.87hr - $42.87hr
- May be responsible for coordinating the display of graphics and the production of the document.
- Writes a variety of technical articles, reports, brochures, and 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.
Skills :
- Familiar with a variety of the field 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.
Education :
- Bachelor's Degree.
- Technical writing certification preferred.
- 2 years relevant experience in the pharmaceutical, biotech, medical device, or other regulated environment.
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