الوصف الوظيفي
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’sPrivacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.Job DescriptionJob Title: Vaccine External Supply Quality Lead, AsiaLocation: Singapore OR Gurgaon, IndiaAbout the role:Accountable and responsible for creating and leading an appropriate Quality oversight organization and for designing, establishing and continuously improving a Quality Management System which ensures consistency in achieving process and product quality and compliance across multiple local Contract Organizations (CMOs, Contract Testing Organization, Distribution Organization) for clinical trial and commercial material. Responsible for critical quality and compliance decisions regarding locally manufactured, tested vaccine products for local and global distribution. In close collaboration with internal teams such as Vaccine Operations, Regulatory Affairs, and Legal team. This role negotiates contracts, and establishes policies with external contract organizations. Planning and managing functional budget including budget for work packages/activities at contract organization.How you will contributeProvides strategic leadership and has accountability for external manufacturing & testing quality oversight of vaccines in the Asia region. Provides guidance on quality considerations and supports negotiation of contract terms across multiple sources of supply. Establishes & maintains contracts/policies/procedures. Responsible for making critical quality and compliance decisions regarding vaccine process & products manufactured/tested at Asia CMOs, including clinical trial material, commercial material, and starting (cell banks and virus banks) material.Drives collaboration with external partners in Asia to assure consistency in achieving process / product quality and compliance across multiple Contract Manufacturing Organizations (CMOs).Ensures product supply, compliance with local regulatory requirements, and global vaccines dossier in partnership with local cross functional internal partners for external supply, Regulatory Affairs, project management, process development and VBU Quality and Global Quality and regulators.Builds and leads the local QA team. Creates, develops, deploys and maintains an adequate and effective QMS system. Ensures timely execution of Quality Assurance and Quality Operations tasks and appropriate cGMP oversight to ensure successful tech transfer and subsequent commercial supply continuation. Shapes the long-term strategy and framework for vaccines External Supplier Quality in the region; including day to day operations such as review & approval of batch records, investigations, documents, change control, submission of batch specific documents to local authorities, batch disposition, process and analytical method performance monitoring and trending.Establishes, maintains, and monitors supplier files including Quality Agreements with CMOs and their suppliers. Plans, creates, and controls the department budget and budget related to CMO quality work-packages, aligns financial planning with strategic global VBU quality objectives & budget plan with Vaccines Operations partners.Act as the key-quality lead for CMO´s Site Quality Head and Senior Quality management team regarding vaccine operations executed at local CMOs and as the key quality partner for internal VBU and Takeda functions regarding vaccine manufacturing, testing, and supply in Asia, for Pan American Health Organization countries and for World Health Organization.Ensure cGMP requirements, Takeda expectations, and global dossier compliance are fulfilled for activities at contract facilities.Evaluates, defines and utilizes digital and automation tools to continuously drive operational excellence in collaboration with global functions.Establishes, maintains, and continuously improves system & processes to manage CMO change controls and investigations for issues associated with audits, manufacturing/testing events, and complaints, ensuring appropriate actions are implemented and aligned with VBU global product life cycle management and the company's strategic objectives.Establishes system & processes for manufacturing process and analytical method transfers from Takeda internal sites (or Takeda external partners) to local CMO. Provides quality guidance and oversight for specific tech transfers and ensures execution according to plans and protocols.Designs an appropriate oversight organization model that includes planning of resources to ensure regular representation of QA staff at CMO plant (Person In Plant), packaging site, laboratory, and warehouse/distribution center and leveraging insights to drive performance, strategic decision-making, quality risk management and continuous improvement.Organizes and participates in internal audits. Serves as an expert and key person for regulatory submissions.Enable vaccines national batch release through strong collaboration with local regulator and national control laboratories.Establishes and cascades functional goals based on GQ, VQ and VBU strategy and goals and development plans for the team, focusing on continuous improvement and Takeda’s Leadership Behaviors.Develops & establishes appropriate operating mechanisms with CMOs and with internal interface functions such as joint QCouncils, QRisk Registers, and KPI reviews to manage CMO performance and risk, aligning with the company's strategic objectives and long-term vision.This position interacts frequently with:VBU Quality and VO leadersVBU QA teamGMS QA and QCLOC QARA-CMC (VBU)Local RAVBU Manufacturing Science QualityGlobal Pathogen Safety TeamCorporate alliance partners and Takeda distribution partnersContract Manufacturing Organizations and Contract Testing FacilitiesSupply managementProduct Development, CMC Team LeadersNational Control Laboratory and country MoHsWhat you bring to Takeda:Education and Experience RequirementsBachelor’s Degree or higher in Chemistry, Microbiology, or Life Sciences, or equivalent scientific discipline.Minimum of 7 years’ experience in quality assurance within the pharmaceuticals, biologics, vaccines experience preferredManagement experienceGood Manufacturing Practice experience, or experience in other regulated industry.Excellent communication skills both oral and written.Experience with supporting product inspections from global Regulatory Authorities such as WHO is required.Experience in tender business and requirementsExperience in support of Tech Transfers and subsequent licensure for commercialization is requiredEffectively represent Quality Assurance, both internally and externally.Experience in routine Microsoft Office software packages and specialized software applications as appropriate.Exhibit and promote Takeda Core CompetenciesKey Skills and CompetenciesEquip with good knowledge of quality systems.Equip with good knowledge in the various regulatory requirements.Equip with good presentation skills.Able to solve problems in a logical manner with timely solutions.Able to interact and communicate with all types of personalities in an effective and diplomatic manner.Project management skills is preferred.Product release knowledge is preferred.Be a delegate for QA line manager in his/her absence and approve any QA related documents.Travel 30%LocationsIND - GurgaonWorker TypeEmployeeWorker Sub-TypeRegularTime TypeFull time
