QA Document Control Specialist - cGMP Cell Therapy
TechDigital Group
An established industry player is seeking a Quality Assurance Document Control Associate Specialist to support cGMP Document Control operations. This role involves managing an electronic document system, ensuring compliance with policies and procedures, and supporting audits and inspections. The ideal candidate will have strong communication skills, a background in document control, and the ability to work collaboratively across departments. Join a dynamic team where your contributions will enhance quality systems and ensure regulatory compliance in a fast-paced environment. This is a fantastic opportunity for those looking to make a significant impact in the quality assurance field. #J-18808-Ljbffr
Vacancy posted 23 hours ago
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