Technical Writer (GMP)
About this role
Technical Writer (GMP)
Yoh is hiring a Technical Writer (GMP) for our Pharmaceutical Manufacturing client in St. Louis, Missouri Essential Job Functions: Must maintain operational compliance with US and international regulatory agencies and guidelines (i.e. FDA, DEA, EU, HC, TGA, RIC/S, ISO, USP, NRC, cGMP, etc.) Manage project submissions as assigned by Director Regulatory Affairs including department work process. Manage key projects, planning, timing, and execution for submission, approval, and launch. Maintain project database for tracking individual and department project deliverables. Manage incoming requests through logging, assigning, tracking, working with RA staff to manage complexity and difficulty, and maintain department metrics.
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