Document Control/QA Coordinator (Mastercontrol)

Monogram, part of LabCorp''s Specialty Testing Group, is seeking a Quality Coordinator to join its team in South San Francisco! As an integral member of the Quality department, this position will be responsible for the overall support and maintenance of Monogram''s controlled documents and the continuous assessment/improvement of related systems and processes to ensure compliance with applicable regulatory requirements. Previous document control and experience with MasterControl or similar systems highly desired! The schedule for this position will be: Monday-Friday, 8am-5pm.Please note: this position is required to work onsite. This is not a remote role. Responsibilities:Provide maintenance of Monogram''s controlled documentation systems including its electronic documentation system (MasterControl), controlled document master files, controlled document manuals (SOP Binders) and associated processes required for the effective maintenance and continued improvement of the document control system.Responsible for the processing and technical editing of controlled documents including: SOPs, Forms, Tickets, Process Flows, Policies, Validation Protocols and Reports and other controlled documents.Effective management of the documentation requirements for projects and high-priority company goals/plans. Perform comprehensive analysis of documentation requirements and collaborate closely with key document reviewers from various cross-functional groups to ensure efficient and timely approval of all required documents using the MasterControl system.Participate in QA group planning and goal setting. May also provide training and support to other QA groups.Participate in the development of Quality Initiatives and the execution of Monogram''s Quality programs, including: internal audits, client or sponsor audits, personnel training files audit and trending/reporting of quality metrics.Primary support for the Monogram Audit (Host) Team; coordinating with other functional areas to obtain materials, documents, records and other similar references requested during audits and inspections.Requirements: Associates. degree in a scientific discipline with minimum 1 year experience required ORBachelors degree in a scientific discipline with a minimum 1 year experience preferredDocument control/document processing experience in a clinical laboratory, biotechnology environment or other similar industry highly desiredPrevious experience with an Electronic Data Management System (EDMS) such as MasterControl highly desiredMust possess strong technical documentation skillsAbility to function independently within a cross-functional team and address a variety of moderate to complex problems.Excellent (written and verbal) communication and interpersonal skills, solid organizational skills, and ability to contribute to a collaborative, flexible work environment.Knowledge of Quality and Regulatory systemsLabcorp is proud to be an Equal Opportunity Employer:As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant''s race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status.For more information about how we collect and store your personal data, please see our Privacy Statement.

Created: 2025-11-01