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.