Analytical Development Documentation Specialist
Listed on 2026-10-07
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Science
Clinical Research
Cambrex is seeking an AD Technical Writer to generate high quality technical documents—test procedures, protocols, and reports—based on data from the Analytical Development department. Role requires adherence to SOPs, cGMP, ICH, and regulatory guidelines.
You will draft, review, and finalize controlled documents and coordinate approvals using Master Control and Track Wise. Bachelor’s degree in Chemistry and 2+ years in a cGMP lab are preferred.
Join us at Cambrex as our next Analytical Development Documentation Specialist in Charles City, IA, United States.
We are currently recruiting a Analytical Development Documentation Specialist for our team in Charles City, IA, United States.
This is an excellent position to take on the Analytical Development Documentation Specialist role at Cambrex.
As a Analytical Development Documentation Specialist, you will play an important part at Cambrex in Charles City, IA, United States.
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