1:00 PM - 2:00 PM
Senior Product Manager Interview
Sarah Jenkins

2780 Tpc
·3 days ago2780 Tpc
·3 days agoLocation
onsite, Fujisawa, Japan
Commitment
Full Time
Level
Director
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OBJECTIVES/PURPOSE: Establish a clear vision and roadmap for extended characterization that aligns with discovery, development, and manufacturing needs across small and mid molecules (Oligo, small molecules and peptides). Implement, optimize, and apply cutting-edge techniques (e.g., MS, NMR, microscopy) to strengthen understanding of drug substance and product properties, stability, and quality. Identify and integrate emerging technologies and digital tools to modernize characterization platforms and improve efficiency and scientific impact. Create and sustain a high-performing team through hiring, mentoring, resource planning, and talent development. Partner with analytical, DS/DP, manufacturing, and quality teams to ensure characterization insights are embedded into development and production decisions. Build external collaborations and enhance scientific reputation through publications, conferences, and industry engagement.
Deep expertise in mass spectrometry (MS), nuclear magnetic resonance (NMR), and advanced microscopy applied to drug discovery, development, and manufacturing. Ability to generate in‑depth understanding of molecular attributes, structure, stability, and quality for small and/or large molecules across the CMC lifecycle. Oversight of advanced bioassay platforms to support product characterization and performance understanding. Strong grounding in analytical characterization within pharmaceutical CMC, including support of development, scale‑up, and manufacturing. Capability to evaluate, implement, and scale emerging analytical technologies to strengthen characterization depth and efficiency. Experience with crystallography, particle science, and physical chemistry applied to pharmaceutical products. Hands‑on experience implementing modelling, digital tools, and advanced data analytics in characterization workflows. Experience managing external analytical partners and supporting transfer of methods to manufacturing environments. Technical experience supporting regulatory submissions and approval processes from an analytical characterization perspective.
Full authority to define and drive the extended characterization vision, priorities, and roadmap across the CMC portfolio. Autonomy to select, implement, and evolve advanced analytical technologies and digital tools. Decision rights over team structure, hiring, talent development, budgeting, and resource prioritization. Authority to establish external collaborations and set the depth and direction of characterization that informs development and manufacturing decisions.
Work closely with ADQC, DS, DP, manufacturing, and quality teams to align characterization efforts with development and production needs. Provide direction, coaching, and prioritization to internal scientific teams to ensure delivery and capability growth. Engage with senior scientific and functional leaders to shape priorities, strategy, and investment decisions through analytical insight. Build strategic relationships with external partners and represent the organization through publications and scientific forums.
Enterprise and portfolio complexity: Oversight of extended characterization across diverse programs spanning discovery, development, and manufacturing. High scientific and technical complexity: Integration of multiple advanced analytical platforms applied to varied molecules and modalities. Cross‑functional and stakeholder complexity: Managing interdependencies across analytical, DS, DP, manufacturing, quality, and external partners. Change and regulatory complexity: Driving innovation and modernization within a highly regulated, risk‑sensitive environment.
Ph.D. with 5-7+ years, MSc with 10-13+ years, BSc with 12-15+ years of industry experience in a relevant life sciences discipline with in analytical development and characterization. Deep experience with advanced characterization techniques (e.g., MS, NMR, microscopy) applied within CMC. Strong understanding of analytical development supporting discovery, development, manufacturing, and regulatory submissions. Proven scientific leadership, strong communication and collaboration skills, and ability to manage complex priorities and stakeholders. Experience supporting regulatory submissions and approval processes. Track record in modernizing analytical platforms or introducing new technologies at scale.
Proven track record of leading teams, developing talent, and driving strategic initiatives. Strategic thinking: analyses current and future scenarios, disrupts the status quo with innovation, while remaining pragmatic and focused on priorities. Results oriented: Demonstrated ability to drive initiatives from concept to execution. Structured, goal-oriented and highly motivated. Fluent in English. Japanese is a plus. Strong and proven ability to work transversally on a local and global level.
Important Notice concerning working conditions: It is possible the job scope may change at the company’s discretion. It is possible the department and workplace may change at the company’s discretion.
Fujisawa, Japan
Employee
Regular
Full time