Regional Head Regulatory Affairs - APAC

Takeda Pharmaceutical Co.; Singapore; On-site; SGD 550,000 - 750,000; Full time

Job summary

Takeda Pharmaceutical Co. in Singapore is seeking a Regional Head of Regulatory Affairs to provide strategic leadership for APAC, shaping regulatory strategy and ensuring unified execution across LOCs and international leads.

This senior role advances global objectives while accelerating patient access through compliant, timely registrations and lifecycle management. As a member of the leadership team, you will collaborate with global, regional and local stakeholders to harmonize regulatory

Qualifications

• Advanced degree in pharmacy, life sciences, medicine or related field.
• 15+ years of progressive Regulatory Affairs experience in pharma/biopharma, with APAC exposure.
• 8–10+ years in leadership managing multi-country or regional teams.
• Demonstrated track record engaging with national authorities and contributing to regulatory strategy.
• Strong stakeholder management and executive presence.

Responsibilities

• Provide strategic and operational leadership to the APAC RA affiliate network and senior teams.
• Lead regulatory strategy development and execution for drug development projects in APAC.
• Shape and align APAC regulatory strategy with global objectives and harmonize regional execution.
• Represent APAC in regional and global regulatory strategy forums and drive regional voice.
• Oversee regulatory lifecycle management including submissions, variations, renewals, and labeling.
• Build and maintain relationships with national authorities and industry groups.
• Drive harmonization of processes, roles, and quality standards across APAC RA.
• Ensure compliance and inspection readiness across the region.
• Partner with cross-functional teams to enable product launches and lifecycle management.
• Lead regulatory intelligence and anticipate changes to inform strategy and risk mitigation.
• Attract, develop and retain regulatory talent; manage APAC budget and governance.

Skills

Leadership experience

APAC regulatory affairs

Regulatory strategy

Stakeholder management

Executive presence

Education

Advanced degree (PhD/PharmD/MD/MSc) or equivalent

Job description

Job Description

About this role:

The Regional Head Regulatory Affairs, APAC provides strategic leadership for the Regulatory Affairs organization across APAC, leading LOC Regulatory Affairs Heads and International Regulatory Leads to ensure a unified regional voice and effective execution of global regulatory strategy.

The role shapes and drives APAC regulatory strategy, accelerating patient access, enabling successful registration and lifecycle management, and ensuring regulatory compliance. Working closely with global, regional and local stakeholders, the Regional Head brings APAC affiliate and health authority perspectives into enterprise decision-making and translates strategic priorities into consistent regional execution.

As a senior member of the International Regulatory Affairs Leadership Team, the role builds a high-performing, forward-looking organization aligned with Takeda’s business and portfolio objectives, Takeda-ism and the Patient-Trust-Reputation-Business principles.

How you will contribute:

• Provide strategic and operational leadership to the APAC Regulatory Affairs affiliate network (LOC / groups Heads RA and their teams) – setting direction, goals and standards and ensuring optimal performance and professional development.

• Accountable for regulatory strategic proposal and tactical leadership (including implementation) for drug development projects in responsible Area, including but not limited, to health authority interactions, regulatory submissions and other regulatory requirements in line with corporate objectives and timelines in collaboration with International Regulatory Leads (IRL) supporting APAC region team and relevant stakeholders.

• Define, shape, align and ensure execution of the APAC regulatory strategy in line with the global Regulatory Affairs strategy, ensuring a single, harmonized regulatory voice across all APAC affiliates,

• Represent the APAC Regulatory Affairs in regional and global regulatory strategy forums; ensuring the regional perspective to enterprise regulatory strategy is considered regarding portfolio prioritization and operating-model decisions (“voice in regional strategy”).

• Ensure a single, consistent regulatory voice for APAC within global regulatory affairs in close partnership with the Therapeutic Area Units and Marketed Product Development

• Build and maintain effective & strategic relationships with the national competent authorities, and industry associations.

• Drive harmonization of ways of working, roles and responsibilities, processes and quality standards across the APAC RA organization in alignment with International Regulatory Affairs ways of working..

• Provide oversight of regulatory lifecycle management delivered through the affiliates across the APAC portfolio – marketing authorization applications, variations, renewals, labeling and product information – ensuring timeliness, quality and compliance.

• Ensure regulatory compliance across the region and maintain audit and inspection readiness in accordance with national legislation and internal guidelines.

• Partner with APAC business leadership, Medical Affairs, Market Access, MCE, Pharmacovigilance, Quality and Supply Chain & partners ( where relevant) to enable successful product launches, life-cycle management and patient access, aligned with commercial priorities.

• Lead regional regulatory intelligence: anticipate and assess changes in the APAC regulatory environment and translate implications into progressive regulatory strategies, risk mitigation plans and business recommendations.

• Attract, develop and retain regulatory talent; build capability, succession and engagement across the APAC affiliate RA organization and International Regulatory Leads (IRL) supporting APAC region.

• Plan and manage the APAC affiliate Regulatory Affairs budget and resources in coordination with Finance and functional leadership.

• Establish governance, key performance indicators and reporting for the APAC RA organization, reporting into the International Regulatory Affairs Leadership Team.

Regional & enterprise leadership

• Serve as a member of the International Regulatory Affairs Leadership Team and act as senior escalation point for significant regulatory risks and issues arising in APAC.

• Serve as the central point of regulatory contract for the commercial Area

• Sponsor and lead regional regulatory transformation and operating-model initiatives (e.g., LOC integration and harmonization of the APC RA model).

• Represent Takeda in relevant APAC and cross-industry regulatory initiatives and external engagements.

• Ensure the APAC affiliate & IRL organization operates in compliance with Takeda’s values, and all applicable ethics and compliance requirements.

Preferred Qualifications:

• Advanced degree (PhD, PharmD, MD, MSc or equivalent) in pharmacy, life / natural sciences, medicine or a related discipline.

• 15+ years of progressive Regulatory Affairs experience in the pharmaceutical / biopharmaceutical industry, including substantial experience in the APAC environment.

• 8–10+ years of leadership experience managing multi-country or regional teams, ideally across affiliate / LOC organizations.

• Extensive expertise in APAC regulatory affairs .

• Proven senior-leadership training and experience in people and organizational management.

• Continuous professional development in regulatory affairs, legislation and internal guidelines.
• Demonstrated track record of engagement with national competent authorities and of contributing to regional / global regulatory strategy.
• Experience leading through a matrix and driving change across a complex, multi-cultural organization.
• Enterprise leadership, strategic thinking and the ability to influence at senior levels internally and externally.

• Strong stakeholder management, communication and executive presence.

• Ability to build, align and inspire high-performing teams across cultures and geographies.

• Deep understanding of the evolving EU regulatory landscape and its business implications.

• Excellent written and spoken English; additional APAC languages an advantage.

Locations

Singapore, Singapore

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time