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Job Description Role Objectives: • Provide Medical and scientific review expertise across MLR and cMLR processes, ensuring content is scientifically accurate, balanced, evidence-based, compliant, and aligned with approved data, product information, and scientific evidence in the literature. • Serve as a key Medical reviewer and scientific advisor to content-development, Medical Communications, Congress, and Content Factory teams, enabling the development of high-quality, review-ready content and efficient approval pathways. • Partner with Medical, Regulatory, Legal, Compliance, and cross-functional stakeholders to drive consistency, quality, and operational excellence across global content review and approval activities. Key Responsibilities: Medical & Scientific Review • Conduct Medical and scientific review of promotional and non-promotional content, including Commercial, Medical Affairs, congress, digital, and field-facing materials, to ensure accuracy, balance, consistency, and alignment with approved data, product labeling, and scientific evidence in the literature. • Evaluate scientific statements, references, data presentation, and clinical context for appropriateness and supportability. • Provide clear, actionable, and scientifically grounded review feedback. • Serve as the designated Medical reviewer within MLR and cMLR review processes for assigned therapeutic areas, brands, or content portfolios. Content Factory Scientific Partnership • Partner with Content Factory teams and stakeholders to provide scientific guidance throughout content planning, development, and review activities. • Advise on evidence requirements, scientific statements (Medical) and claims (commercial) substantiation, scientific communication objectives, and communication of clinical data. • Support development of reusable and globally scalable content by promoting consistency in scientific communication and evidence utilization, aligned with the approved Scientific Communication Platforms and Lexicons for related assets. • Identify and proactively address scientific-review risks to enhance content quality and review readiness. Cross-Functional MLR/cMLR Collaboration • Participate in MLR/cMLR review discussions requiring scientific expertise and Medical judgment. • Provide clear direction to project owners during the end-to-end lifecycle of the review, starting at the concept review stage until final approval for dissemination. • Collaborate with Medical, Regulatory, Legal, Compliance, Commercial, Scientific Communications, and Content Operations stakeholders throughout the content-review lifecycle. • Support resolution of scientific-review comments and content-related questions. • Partner with MLR Operations teams to drive efficient and consistent review processes. Scientific Excellence & Continuous Improvement • Maintain current knowledge of assigned therapeutic areas, products, treatment guidelines, and emerging scientific evidence. • Ensure Medical-review activities comply with applicable regulations, policies, and procedures. • Contribute to Medical-review standards, best practices, guidance, and capability-building initiatives. • Identify opportunities to improve content quality, review-cycle efficiency, and consistency across review activities. Qualifications: Experience: More than 7 years of relevant experience in the biopharmaceutical, healthcare, Medical Affairs, or Medical Communications industry, including at least 5 years supporting Medical review, MLR/cMLR, Medical Communications, or other regulated content-review activities. Experience collaborating with Medical, Regulatory, Legal, Compliance, and Commercial stakeholders; exposure to global or multi-market review environments and diverse content types is preferred. Technical skills: Strong understanding of Medical review principles, MLR/cMLR processes, and regulated content-development practices. • Ability to communicate complex scientific information clearly to both scientific and non-scientific audiences. • Ability to critically evaluate clinical data, scientific literature, references, and evidence-based claims. • Knowledge of pharmaceutical regulations, compliance requirements, publication standards, and scientific communications. • Experience with Veeva Vault PromoMats, MedComms, iEnvision, or similar review platforms preferred. • Strong communication, stakeholder management, collaboration, and influencing skills. • Strong attention to detail with the ability to manage multiple concurrent review activities. Education: Advanced degree in Medicine, Pharmacy, Life Sciences, Public Health, Medical Communications, or a related scientific discipline required; PharmD, MD, MBBS, PhD, or equivalent advanced scientific qualification strongly preferred. Languages: Fluent English required; additional languages advantageous Locations IND - Bengaluru 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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