Technical Writer — GMP, SOP & Validation
Listed on 2026-10-11
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Quality Assurance - QA/QC
Regulatory Compliance Specialist -
Pharmaceutical
Regulatory Compliance Specialist
Global Channel Management is seeking a Technical Writer to develop validated documentation for pharmaceutical and manufacturing systems. The role requires translating complex software functions into clear, process-driven materials to support implementation and training of applications.
Requires a Bachelor’s degree in a technical field and a minimum of two years’ industry experience, with familiarity in GMP, SOP, validation concepts, and regulatory compliance.
We would love to welcome a new Contract Technical Writer — GMP, SOP & Validation to our group in Rocky Mount, NC, United States.
Full responsibilities and requirements are described in the listing above.
Learn more about the Contract Technical Writer — GMP, SOP & Validation role in the description above.
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