QA Document Control Specialist, cGMP Records

An established industry player is seeking a Quality Assurance Document Control Associate Specialist to support cGMP operations. In this role, you will be responsible for managing GMP records, ensuring compliance with regulatory standards, and facilitating the document approval process. The ideal candidate will have a strong background in document control within regulated environments and possess excellent communication and project management skills.

Join a dynamic team where your contributions will enhance quality and efficiency in a fast-paced setting, making a significant impact on the organization's success.
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