Technical Writer: GMP & Medical Device Docs

Edwards Lifesciences in Irvine, CA seeks a Technical Writer to create GMP protocols, reports, and technical summaries, collaborating with production, regulatory, and management to ensure accuracy and clarity. You will maintain standardized documentation and review content for style, grammar, and consistency.
The role requires a Bachelor's degree in a related field and 3+ years of technical writing experience, with strong editing and communication skills.

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