GMP Document Control Specialist

An established industry player is seeking a Manufacturing Tech Writer to support operations by managing document revision workflows and ensuring compliance with quality standards. This role involves collaborating with cross-functional teams, overseeing document change requests, and participating in audits and regulatory inspections. The ideal candidate will have a strong background in document management within a cGMP/FDA regulated environment, excellent communication skills, and a commitment to quality improvement.

Join a dynamic team where your contributions will enhance manufacturing processes and drive operational excellence.
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