QS Document Control Specialist

Role Overview: Supporting the implementation and sustainability of Document Control and Change Management programs at a manufacturing site. The position involves facilitating change approval processes, maintaining quality documentation within the Quality System, and ensuring compliance with customer, regulatory, and company standards. Key Responsibilities Monitor and ensure only validated changes are incorporated into product documentation.Train new employees and internal stakeholders on processes.Collaborate with departments for timely change control implementation.Facilitate procedure updates and route documents for review and approval.Manage site periodic reviews, document filing, archiving, and retrieval.Support internal and external audits and quality projects. Qualifications & Skills Bachelor’s degree in a STEM field, or related discipline, or 4 years of relevant experience.No prior experience required; 2 years in a GMP environment preferred.Proficiency in MS Office; experience with TrackWise Digital and SAP is a plus.Strong attention to detail, communication skills, and ability to multitask.Ability to walk within campus, lift objects up to 50 pounds, and adapt in a fast-paced environment.