Remote CMC Technical Writer — Regulatory & Analytical Expert
Boston, Suffolk County, Massachusetts, 02298, USA
Listed on 2026-10-07
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Research/Development
Clinical Research, Medical Science
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.
We are currently recruiting a Remote CMC Technical Writer — Regulatory & Analytical Expert for our team in Boston, MA, United States.
Learn more about the Remote CMC Technical Writer — Regulatory & Analytical Expert role in the description above.
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