Quality Management System (QMS) Document Control Specialist

Flex is the diversified manufacturing partner of choice that helps market‑leading brands design, build and deliver innovative products that improve the world. A career at Flex offers the opportunity to make a difference and invest in your growth in a respectful, inclusive, and collaborative environment. If you are excited about a role but don’t meet every bullet point, we encourage you to apply and join us to create the extraordinary. General Purpose Responsible for supporting the QMS Document Control Supervisor in the controlled management of QMS documentation, including the logging, distribution, revision, control, storage, retrieval and maintenance of electronic and hardcopy quality documents (e.g. Policies, Procedures, Work Instructions, Forms) in compliance with FDA and ISO requirements. Accountabilities Support the QMS Document Control Supervisor in daily document control activities. Maintain controlled QMS documentation in accordance with approved procedures and regulatory requirements. Ensure documents are properly reviewed, approved, released, revised, and archived within the eQMS. Support Change Control activities for QMS documents, including tracking revisions and approvals. Assign document control numbers and maintain accurate version history, status, and traceability. Ensure document release packages are complete, accurate, and current. Support records control activities, including retention, retrieval, and audit readiness. Support internal, external, ISO, and FDA audits by retrieving documentation and providing objective evidence. Assist in continuous improvement initiatives related to document and configuration control processes. Collect and report document control metrics (e.g., review cycle times, on‑time release). Proactively support department objectives and performance targets. Minimum Qualifications High School Diploma or equivalent technical training. 5+ years of experience in document control within a regulated (FDA/ISO) manufacturing or quality environment. Strong understanding of FDA 21 CFR Part 820/QMSR, ISO 13485, and Good Documentation and Manufacturing Practices (GDP/GMP). Demonstrated experience managing the document lifecycle (creation, review, approval, release, revision, archiving). Hands‑on experience with electronic Quality Management Systems (eQMS) (e.g., ComplianceQuest, Agile). Proficiency with Microsoft Office (Word, Excel, PowerPoint) and document formatting using approved templates. Equivalent combinations of education, experience, and certifications will be considered. Flex is an Equal Opportunity Employer and employment selection decisions are based on merit, qualifications, and abilities. We do not discriminate based on age, race, religion, color, sex, national origin, marital status, sexual orientation, gender identity, veteran status, disability, pregnancy status, or any other status protected by law. We're happy to provide reasonable accommodations to those with a disability for assistance in the application process. Please email View email address on click.appcast.io and we'll discuss your specific situation and next steps. #J-18808-Ljbffr Flex