Title: ADQC Technical Writer
This position can be full time remote, 1-2 on site visits/month
Contract duration: 6 months, with possible extension
Day Shift, Monday to Friday, 8:00am to 4:30pm
This position is a 6 month position supporting analytical transfer documentation in the Analytical Development and Quality Control department. This position supports the Analytical Development team in the cell and gene therapy division of Genentech, authoring and reviewing documents such as method validation protocols, reports, test methods, and SOPs, while ensuring GMP standards are met.
You are responsible for working closely with relevant stakeholders as well as cross-site SMEs to draft, review and approve technical documents.
Job Duties/Responsibilities:
Author and edit a wide range of technical documents, including but not limited to:
Job Qualifications:
You will stand out if you have:
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