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’s Privacy 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 Description PV Area Lead, Southeast Asia & India (SEA-I) Location: India Southeast Asia and India are among the most diverse and dynamic pharmacovigilance environments in the industry. In this role, you'll set the pharmacovigilance strategy for the Area and lead the Local Patient Safety teams, keeping patient safety at the centre of how Takeda operates in every market. As the Area's main point of contact for safety matters and escalations, you'll work in close partnership with Global and Regional PSPV colleagues. You'll report to the PSPV Head, Asia Pacific, Middle East & CIS, as part of Patient Safety & Pharmacovigilance Affiliate Management (PSPV-AM) within R&D Data and Quantitative Sciences. How You Will Contribute Strategy & Leadership Define and lead the Area PV strategy, aligned with global and regional PSPV direction Set the Area's goals, KPIs and long-term plans, and build the PV capabilities needed to deliver them Lead and develop the Local Patient Safety teams, and build career paths for the next generation of PV talent Build strong, inclusive matrix partnerships across R&D and Commercial Compliance & Quality Be accountable for quality management and for PV compliance with local, regional and global post-marketing safety regulations across all countries and clusters Lead audit and inspection readiness and oversight, with Global PV Compliance and Takeda Quality Keep processes aligned and training compliance high, working with PSPV Compliance, Training and Alliance Operations & Resources Support the Area's PV budget, resourcing model and vendor partnerships Anticipate regulatory change and lead how processes adapt across the Area External & Internal Partnership Act as the Area's senior contact for safety issues and escalations, and as PV contact for the Health Sciences Authority (HSA) in Singapore, if applicable Serve as deputy Qualified Person for Pharmacovigilance (QPPV) or backup PV manager where needed Escalate to the Regional Head, and keep Medical Affairs, Regulatory Affairs, Quality Assurance and Compliance aligned on PV matters Partner with the PSPV-AM Patient Access and Vaccines Lead and Patient Access Programmes, and on vaccine safety discussions with National Health Authorities Skills and Qualifications Bachelor's degree required. An advanced degree in healthcare, life sciences or medicine is preferred. At least 10 years of pharmaceutical industry experience, including line management, with significant exposure to drug safety, clinical operations, R&D project management and local affiliates Advanced knowledge of PV operations, global safety regulations and business planning Proven leadership in building and developing high-performing teams across countries A track record of leading large-scale change, multi-country projects and timely decisions on complex matters Strong analytical skills, with the ability to turn complex data into clear priorities Strong influence in a matrix organisation, with excellent communication skills and the presence to represent PSPV inside and outside the company Fluent English. Other languages are an advantage. Professional Scope and Leadership Director-level role with a high degree of autonomy across a broad, multi-country Area Complex, high-impact decisions affecting patient safety and Takeda's regulatory standing, with influence that reaches senior stakeholders and health authorities Why Join Us At Takeda, our values of Patient, Trust, Reputation and Business guide every decision. In this role, you'll shape pharmacovigilance across a fast-growing Area where regulations keep changing, with the backing of one worldwide PSPV team. If you're ready to lead pharmacovigilance at this level, we would welcome your application. Benefits It is our priority to provide competitive compensation and a benefit package that bridges your personal life with your professional career. Amongst our benefits are: Competitive Salary + Performance Annual Bonus Flexible work environment, including hybrid working Comprehensive Healthcare Insurance Plans for self, spouse, and children Group Term Life Insurance and Group Accident Insurance programs Health & Wellness programs including annual health screening, weekly health sessions for employees. Employee Assistance Program 5 days of leave every year for Voluntary Service in addition to Humanitarian Leaves Broad Variety of learning platforms Diversity, Equity, and Inclusion Programs No Meeting Days Reimbursements – Home Internet & Mobile Phone Employee Referral Program Leaves – Paternity Leave (4 Weeks) , Maternity Leave (up to 26 weeks), Bereavement Leave (5 days) About ICC in Takeda Takeda is leading a digital revolution. We’re not just transforming our company; we’re improving the lives of millions of patients who rely on our medicines every day. As an organization, we are committed to our cloud-driven business transformation and believe the ICCs are the catalysts of change for our global organization. Locations IND - Bengaluru Worker Type Employee Worker Sub-Type Regular Time Type Full time Locations IND - Bengaluru - Research and Development Worker Type Employee Worker Sub-Type Regular Time Type Full time Locations IND - Bengaluru Worker Type Employee Worker Sub-Type Regular Time Type Full time Locations IND - Bengaluru Worker Type Employee Worker Sub-Type Regular Time Type Full time Locations IND - Bengaluru - Research and Development Worker Type Employee Worker Sub-Type Regular Time Type Full time Takeda is an industry-leading, global pharmaceutical company with an unwavering dedication to putting patients at the center of everything we do. We live our values of Takeda-ism – Integrity, Fairness, Honesty, and Perseverance – and are united by our mission to strive towards Better Health and a Brighter Future for people worldwide through leading innovation in medicine. Here, everyone matters and you will be a vital contributor to our inspiring, bold mission. At Takeda, you will make an impact on people’s lives – including your own. Takeda is an equal opportunity employer. For applicants of U.S and Puerto Rico positions: Click here to learn about our commitment to Equal Employment Opportunity (EEO). If you are limited in the ability to use our job application tool, or otherwise require a reasonable accommodation for a disability please click here.

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