Quality Control Specialist

We are seeking an experienced Documentation (QC) Specialist to support quality documentation, specifications, methods, and change control activities within a pharmaceutical manufacturing environment. This role will be responsible for reviewing and maintaining commercial testing methods, specifications, and global testing standards while ensuring compliance with cGMP and regulatory requirements. Key Responsibilities Review, manage, and maintain commercial specifications, analytical methods, and supporting QC documentation Perform content review and quality approval of change controls, testing standards, and method documents Support creation, revision, and lifecycle management of specifications and testing methods Maintain document management systems and ensure accurate document control practices Manage Global Testing Standards (GTS) documents, notifications, and document obsolescence activities Support change management initiatives and ensure compliance with quality and regulatory requirements Collaborate with QA, QC, Regulatory, Manufacturing, Stability, Supply Chain, and R&D teams Qualifications 4+ years of Pharmaceutical, Biotech, or related industry experience Strong knowledge of QC methods, specifications, compendial requirements, and cGMP regulations Experience with document management systems, change controls, and quality documentation Familiarity with SAP, LIMS, or related laboratory systems preferred Strong attention to detail, communication, project management, and cross-functional collaboration skills #J-18808-Ljbffr United Pharma