One of our large pharmaceutical clients is actively hiring for a Technical Writer for a new manufacturing building, that supports Live Virus Vaccine Manufacturing Filling. The Technical Writer will be responsible for completing the revision of 150 SOP documents for formatting and consistency. You will be working with the Operations, Manufacturing and Engineering subject matter experts to review the SOPs, understand what needs to be updated, complete redlining, formatting & grammatical edits, & then the Technical Writer will be using MS Word to make the edits and submit through the document revision process. Examples of formatting you will be required to review are alignment of bulleting, pictures, making sure pictures are readable, font & font sizes are consistent, etc. You will be trained in their internal document management system process. This is a fully remote position, working part-time around 20 hours per week.
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- 3-5+ years of Technical Writing experience within a GMP manufacturing environment
- Experience reviewing, editing, and improving SOPs in MS Word
- Previous biotech/pharmaceutical industry experience
Self-starter with the ability to manage individual project timelines with minimal oversight
Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.