Quality Assurance Specialist - Pharmaceuticals

## Overview #### **Company Overview** WuXi STA is building new pharmaceutical manufacturing capability and is establishing the quality systems that will support it. For more information, see: New manufacturing facility announcement About the company ## Responsibilities The Quality Assurance Specialist is a fully qualified quality professional who provides independent, on-the-floor quality assurance support to manufacturing and operations while the site’s GMP quality system is being established. This is a build role rather than a maintenance role: the Specialist helps stand up the quality processes, systems, and documentation required for Oral Solid Dosage (OSD) and Sterile drug-product manufacturing—including aseptic processing and drug-substance operations—and ensures compliance with applicable GMP regulations and health-authority expectations. Working with limited precedent, the Specialist exercises independent judgment to resolve quality issues of diverse scope, advises operations and cross-functional partners, and helps embed a “Right First Time” culture as the site progresses toward routine GMP operations. Work is performed independently and reviewed at critical points. ## Key Responsibilities - Provide independent on-the-floor quality assurance support to manufacturing and operations, including real-time batch record review and timely disposition of quality events during production. - Help establish and document the site quality management system (QMS), authoring and improving SOPs, work instructions, and job aids for sterile/aseptic and drug-product operations to meet FDA, EMA, and other applicable health-authority requirements. - Own quality events end to end—deviations, investigations, root-cause analysis, CAPAs, change controls, and effectiveness checks—applying structured problem-solving to events of diverse scope and limited precedent. - Review commissioning, qualification, and validation (CQV) documentation, including URS, FAT/SAT, turnover packages, IQ/OQ/PQ, and process validation. - Lead readiness inspections of manufacturing areas, equipment, computerized systems, and processes to identify and mitigate quality risks prior to operational start-up. - Support new product introduction (NPI) and technology-transfer activities, providing quality oversight of batch records, bills of materials, and related documentation to enable right-first-time execution. - Design and deliver quality and GMP training, and coach operations and quality colleagues to build capability and a sustained “Right First Time” culture during this formative period. - Serve as a quality subject-matter expert for internal, client, and regulatory inspections, and advise stakeholders toward sound and compliant decisions. - Ensure complete, accurate, and contemporaneous records in accordance with Good Documentation Practices and data-integrity (ALCOA+) principles, including appropriate use of electronic QMS and document-management systems and other validated digital quality tools. - Partners across manufacturing, engineering, and validation functions to integrate quality requirements into daily operations. ## Qualifications - Bachelor’s degree in scientific or engineering discipline, or an equivalent combination of education and directly relevant experience. - Approximately five years of pharmaceutical or biopharmaceutical quality assurance experience, or an equivalent combination of education and directly relevant experience, including hands-on time in a GMP manufacturing environment. - Experience supporting a greenfield site or new-facility start-up and standing up QMS processes from the ground up, or experience with New Product Introduction (NPI). - Experience working in a multiproduct pharmaceutical manufacturing facility, including managing differing customer requirements and the controls used to prevent cross-contamination between products. - Demonstrated, hands-on understanding of both manufacturing/production operations and quality assurance…