Senior Technical Writer — FDA‑Regulated GMP Docs

A life sciences professional services company is seeking a Technical Writer to produce high-quality documentation in FDA-regulated environments. Responsibilities include authoring SOPs and collaborating with experts across various teams. Candidates should have a bachelor's degree and at least five years' experience in technical writing. Exceptional communication skills and a detail-oriented approach are essential.

This role offers an opportunity to impact patient safety positively while working in a dynamic team environment.
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