Director Quality Assurance Manufacturing
: Job Details :

Works closely with Quality Assurance Management, Quality Assurance Managers and support functions in providing direct oversight and leadership in the support of Late Phase and Commercial Manufacture of Cell Therapy Products according to current Good Manufacturing Practices (cGMPs). Direct department employees, resources and programs to ensure compliance with all regulatory requirements; specifically Good Manufacturing Practice (cGMP), Code of ederal Regulations (CFR), EU Guide to Good Manufacturing Practice, International Conference on Harmonization (ICH), Good Tissue Practices (GTP) and relevant foreign regulatory guidelines for biopharmaceuticals. Ensure compliance of critical functions for the site, monitor, trend and report on all aspects of Quality by workingIdentify, implement and drive quality improvement projects and policies to reflect industry best practices.Direct and lead staff in support of the commercial manufacturing, testing, andrelease of Cell Therapy Products in compliance with Regulatory Applications andIndustry Regulations.Direct and lead employees within quality assurance and cross-functionally toensure active maintenance in keeping the site current with changes to GXP,including FDA and EU and other relevant foreign regulatory bodies as well asguidance documents (ie: ICH, PTC, ISPE, etc.).Drive continuous improvement and execute pro-active quality control in site'sprocesses.Accountable for ensuring that investigations are completed in a thorough andtimely fashion in order to meet customer commitments and comply with regulatoryexpectations.Direct and Manage QA support for site quality systems such as Change Controls,Investigations, Corrective and Preventive Actions, and Product QualityComplaints.Lead and participate in site quality and process improvement initiatives, and project teams.Provide compliance support, expertise and training for the site. Provide direct andimmediate support for internal, external and regulatory audits of site.Oversee compliance-critical functions including change control, validation andcompliance and quality improvement projects.Develop, implement and approve QA policies and procedures.Establish and maintain a closed loop management process that drives continuousimprovement in performance to objectives and fact based decision makingIn collaboration with the site management, set strategic direction for current andfuture product, systems, work practice, and process improvementsProvide leadership in directing the efforts of management, supervisory and directlabor for the QA Department.Direct, oversee and participate in the recruitment, selection, promotion, terminationand performance management of QA personnel.Foster a spirit of collaboration, cooperation, honesty, and integrity while remainingflexible with customer focus.Ensure the quality management systems are implemented to ensure a consistentlevel of quality and compliance in all processes. Monitor and maintain qualitysystems and procedures (SOPs) for adherence to regulatory compliancerequirements. Focus on driving continuous compliance and quality improvements.Develop, implement and approve QA policies and procedures.Support the site in compliance-critical functions including Non-conforming Events,Laboratory Investigations, Change Control, Document Management and CAPAsystems and processes.Review, approve and perform investigations and provide guidance for CAPArelated to non-compliance situations using creative problem-solving skills.Lead and/or participate on cross-functional teams and projects representing qualityin positive and compliant manner. Develops, coordinates, and follows organizational systems, policies, procedures,and follows labor and capacity standards.Bachelors Degree required and~10+ years relevant technical experience and min 7 years Managing people~ BS/BA in Science related field preferred; Thorough working knowledge of Regulatory Compliance, Quality SystemManagement and Quality Assurance principles and practices. Strong knowledgeof 21 CFR 210 and 211, 21 CFR Part 11, EU Guide to Good ManufacturingPractice.Experience in the development, streamlining, and optimization of Quality SystemsExperience with Quality Management Systems i.e. Ability to work under limited supervision and to handle complex problems.Proficient in Microsoft (Excel, Word, Outlook)Travel is required 5-10% , Domestic/International, Daily / OvernightOur greatest asset is our people, WuXi is dedicated to providing opportunities for internal growth with direct access to a dedicated and accessible Human Resources team.WuXi AppTec provides equal employment opportunity to all individuals regardless of their race, color, creed, religion, gender, age, sexual orientation, national origin, disability, veteran status, or any other characteristic protected by state, federal, or local law.WuXi AppTec requires all employees, both Field and Office-based, to be fully vaccinated with a COVID-19 vaccine by January 4, 2022. You will be required to upload an image of your COVID-19 vaccine card at the time of hire and/or on your first day of employment.