You will be part of a growing lab support group and an agile team to create a strong, collaborative culture. Prefer 0-2 years of previous document control experience, preferably in a regulated industry. Responsibilities: maintains document and revision information; monitors tasks relating to documents; reconciles and updates each SOP manual; complies with cGMPs and company policies and procedures; supports Document Control Supervisor and QA Director/Manager during client audits; scans files/records/data as needed; files records as needed; prepares files for archive storage; performs other related duties as required. Requirements: High school diploma or equivalent and 0-2 years of experience in the pharmaceutical field or related area; proficiency in Microsoft Word, Excel, Access and other programs; experience with GMP compliance systems (e.g., QMS, change management, ERP) is a plus; experience in a pharmaceutical company preferred; excellent interpersonal and communication skills; ability to solve complex business problems and present recommendations; strong verbal and technical writing skills; results driven, quick learner, and self-starter.