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Associate Director, Development And Medical QA (Asia)

Daiichi Sankyo Singapore Pte. Ltd.

D01 Marina, Raffles Place, People's Park, CecilFull TimeS$12,000 – S$14,000/mo

Posted 3 Jul 2026

About this role

The Associate Director is responsible for driving a proactive approach to operationalize the Development and Medical QA mission and strategy, and work in close collaboration with the Head of Development and Medical QA (Asia Pacific) to translate quality strategy into practical execution, drive risk-based quality oversight, and strengthen quality culture across Asia organization. JOB DESCRIPTION - Act as a trusted QA partner to Clinical and Medical Affairs stakeholders by providing proactive quality advice, risk assessment and oversight. - Instill a consistent mindset and culture through partnering with stakeholders to streamline the product lifecycle process by embedding proactive quality approach. – Quality by Design (QbD) and supporting risk-based decision making, developing risk mitigation strategies across projects and initiatives. - Lead and support inspection readiness and management activities, including acting as Inspection Management Team Lead and coordinating pre- and post-inspection activities. - Lead formal investigations of issues as they arise, ensuring timely escalation to line management if critical incidences are not resolved in due course. - Provide guidance during the root cause analysis and development and execution of Corrective and Preventive Actions (CAPAs). - Collaborate with Head of Development and Medical QA (Asia Pacific) to monitor and analyze quality risks and trends (e.g., quality events, audits, inspections), and drive continuous improvement actions. - Contribute to the enhancement of the local QMS by aligning processes with regulatory requirements, global standards, and evolving business needs. - Provide proactive quality support aligned with business strategy, including consultation and guidance on quality-related concerns, resolution of vendor-related issues identified for the assigned studies. - Execute quality oversight activities by embedding Quality by Design (QbD) principles across the product/clinical trial lifecycle; in collaboration with Head of Development and Medical QA (Asia Pacific) to translating QA strategy into operational practice. - Support implementation of applicable GxP and regulatory requirements in day-to-day activities, ensuring compliance while partnering with stakeholders to address operational needs. - Contribute to the delivery of global and regional QA objectives and strategic initiatives by supporting local execution and aligning with Head of Development and Medical QA (Asia Pacific) priorities and business needs. - Drive implementation of program-specific quality plans, ensuring alignment of business priorities with quality oversight and deliverables. - Lead or support preparation and management of regulatory inspections as assigned by Head of Development and Medical QA (Asia Pacific). - Coordinate pre-inspection activities, including document readiness, stakeholder preparation, training, and mock inspections when applicable. - Act as QA representative and/or point of contact during inspections, supporting interactions with health authorities as appropriate. - Support inspection responses, including observation management, root cause analysis, and CAPA development and follow-up. - Lead or support Quality Event (QE) management activities, including deviation reporting, investigation, root cause analysis (RCA), and CAPA development. - Ensure appropriate escalation, criticality assessment, and tracking of QEs in alignment with QMS requirements. - Support monitoring of QE trends and contribute to continuous improvement through lessons learned and risk mitigation actions Business Partnering. - Act as a key QA partner to local stakeholders (e.g., Clinical, Medical Affairs), providing practical and solution-oriented quality advice. - Serve as a liaison between local teams and global/regional QA functions to ensure alignment and effective communication. - Collaborate with relevant QA functions (e.g., Audits & Compliance, PV/MA QA, QMS) to ensure consistency of quality and compliance activities. - Support implementation and maintenance of the local QMS in alignment with global standards and Head of Development and Medical QA (Asia Pacific) direction in partnership with the relevant business function in DSTW. - Contribute to the development and continuous improvement of local QA frameworks (e.g., QA Manual, Quality Gate processes). - Support monitoring of compliance metrics, evaluate quality risks through analysis of Quality Events, audit and inspection outcome…

What they're looking for

ClinicalProcess ImprovementLeading Development TeamsInvestigation

About Daiichi Sankyo Singapore Pte. Ltd.

Industry: Wholesale & retail tradeWebsite ↗

Frequently asked questions

What does a Associate Director, Development And Medical QA (Asia) at Daiichi Sankyo Singapore Pte. Ltd. do?

The Associate Director is responsible for driving a proactive approach to operationalize the Development and Medical QA mission and strategy, and work in close collaboration with the Head of Development and Medical QA (Asia Pacific) to translate quality strategy into practical execution, drive risk-…

What skills does this Associate Director, Development And Medical QA (Asia) role need?

Key skills for this role include Clinical, Process Improvement, Leading Development Teams, Investigation.

How much does a Associate Director, Development And Medical QA (Asia) at Daiichi Sankyo Singapore Pte. Ltd. pay?

This role lists a salary of S$12,000 – S$14,000 per month.

Is this Associate Director, Development And Medical QA (Asia) role remote, hybrid, or on-site?

The listing is based in D01 Marina, Raffles Place, People's Park, Cecil. Check the posting for remote or hybrid options.

How do I apply for this Associate Director, Development And Medical QA (Asia) role?

You can apply directly on Daiichi Sankyo Singapore Pte. Ltd.'s careers page. ApplyLah can tailor your résumé and cover letter to this exact role in seconds first.