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Job description
Centessa Pharmaceuticals seeks a Contract CMC Technical Writer to critically review data, methods, batch records, and development reports from external CDMOs to finalize source documents for analytical, drug substance and drug product, and to prepare regulatory content and summaries.
You will write scientific content, author conclusions for submissions, and coordinate with Quality, Clinical Supply and Regulatory to align documents for modules and filings; based in the US with remote work.
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Worksite address
boston, MA, 02298, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.