This is a four to six months contract onsite in Foster City, CA. The candidate must be able to commute to the site daily.
- Must have at least three years of technical and procedure writing experience. The work is related to facilities department of biotech / pharmaceutical manufacturing site.
- Prior experience in developing GMP procedures is a plus.
- Understanding biotech / pharmaceutical validation document process is a plus.
- Must have the skills and persistency in following up and solicit the required review comments or information from the very busy stakeholders.
- Excellent communication and professional presence in meeting and note taking skills.
- Computer and typing savvy, experienced in Google suite and Microsoft products in developing, soliciting and incorporating comments.
The work is to finalize two draft procedures related to the electrical maintenance and parts substitutions.
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