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神奈川県の研究職（応用研究員）の求人206件応募資格・募集要項・仕事内容を見る
Principal Scientist, Synthetic Molecules Characterization & Attribute Sciences, Analytical Development
- 給与
- 記載なし
- 勤務地
- 神奈川県
- 休日
- 年間休日123日
- 雇用形態
- 正社員
どんな仕事かAIによる生成
The Principal Scientist independently leads characterization activities for synthetic molecules and supports early-stage developability assessment and candidate selection in collaboration with Research. The role generates and integrates physicochemical, solid-state, stability, and biopharmaceutical evidence, and translates findings into scientific recommendations. It also provides technical expertise across Pharm Sci functions and scientific oversight of CROs and external laboratories.
この求人に応募
応募資格
必須
- Bachelor’s degree in Chemistry, Engineering, Biology, Analytical Chemistry or related Pharmaceutical Science and 7+ years relevant industry experience
- Master’s degree in Chemistry, Engineering, Biology, Analytical Chemistry or related Pharmaceutical Science and 5+ years relevant industry experience
- PhD in Chemistry, Engineering, Biology, Analytical Chemistry or related Pharmaceutical Science and 3+ years relevant industry experience
- Demonstrated ability to independently design studies, integrate data across disciplines, and communicate actionable scientific conclusions.
- Technical knowledge and skills of solid form study, biopharmaceutical assessment and physicochemical profiling of synthetic molecules.
- Understanding of pharmaceutical development and the relationship among candidate properties, material attributes, formulation, process, stability, biopharmaceutics, and analytical strategy.
- Strong scientific judgment, problem-solving, technical writing, presentation, collaboration, and stakeholder-influence skill.
- Experience with in silico tools, predictive modeling, statistics, data science, automation, or AI-enabled scientific workflows.
- Knowledge of analytical techniques with experience in multiple techniques for synthetic molecules such as LC, dissolution, spectroscopy, particle size analysis, XRPD etc.; Able to work in a lab setting and independently interpret results of complex experiments.
- Excellent organizational and communication skills. Has the ability to influence at all levels of the organization and manage projects across businesses and the globe.
- Proven external scientific track record through presentations at scientific conferences and publication of peer-reviewed manuscripts
募集要項最終確認 10/28
- 職種
- 研究職（応用研究員）
- 雇用形態
- EmployeeRegularFull time
- 役職
- Principal Scientist
- 給与
- 記載なし
- 給与の詳細
- Salary Increase: Annually, Bonus Payment: Twice a year
- 手当
- CommutationHousingOvertime Work
- 勤務地
- Fujisawa, Japan
- 転勤
- It is possible the department and workplace may change at the company’s discretion.
- 働き方
- Flextime, Telework
- 勤務時間
- Research Site (Kanagawa) 9:00-17:45Flextime
- 年間休日
- 123日
- 休日・休暇
- SaturdaysSundaysNational HolidaysMay DayYear-End Holidays etc. (approx 123 days in a year)Annual Paid LeaveSpecial Paid LeaveSick LeaveFamily Support LeaveMaternity LeaveChildcare LeaveFamily Nursing Leave
- 福利厚生
- Flextime, TeleworkSocial Insurance, Retirement and Corporate Pension, Employee Stock Ownership Program, etc.
- 社会保険
- Social Insurance
- 業務の変更の範囲
- It is possible the job scope may change at the company’s discretion.
- 就業場所の変更の範囲
- It is possible the department and workplace may change at the company’s discretion.
- 経験年数
- 3年以上
- 学歴
- 大学卒業以上
- 掲載日
- 2026/10/18 10:07（11日前）
- 最終確認
- 2026/10/28 21:15（1日前）
仕事内容
Objectives / Purpose
- Independently leads characterization activities of synthetic-molecule through the strategic planning and execution based on phase appropriate pharmaceutical development.
- Supports early-stage developability assessment and candidate selection in collaboration with Research by physicochemical, solid-state characterization, solid form study, and product-relevant understanding.
- Contribute to pipeline development and strategic discussion to evaluate impact of decisions across PharmSci functions and other development functions through physicochemical, solid state, structural characterization, solid form study, and technical investigations.
- Required to be recognized as a subject matter expert in analytical characterization such as spectroscopic analysis, X-ray analysis, NMR, MS spectrometry, Thermal analysis and other spectrometry for synthetic molecules (Small molecules, Oligonucleotides, Peptides) with the capabilities of data science, in silico modeling for molecular characterization, stability prediction and GI absorption / pharmacokinetic modeling etc.
Accountabilities
- · Lead developability assessments for candidate molecules in collaboration with Research and Pharmaceutical Sciences partners.
- · Generate and integrate physicochemical, solid-state, stability, and biopharmaceutical evidence to identify development risks and enable candidate selection.
- · Translate characterization findings into clear recommendations for candidate selection, developability risk mitigation, solid-form strategy, and formulation direction.
- · Apply solid-state and material techniques, such as XRPD, DSC, TGA, DVS, microscopy, spectroscopy, particle characterization, and related methods; expertise in every technique is not required.
- · Characterize impurities including nitrosamines and mutagenic impurities and contribute scientific evidence to multidisciplinary risk assessments.
- · Lead or support investigations of unexpected analytical observations, material variability, degradation, stability trends, manufacturing events, and product-performance concerns through orthogonal techniques such as NMR, MS, spectroscopy, chromatography, diffraction, thermal analysis, and microscopy.
- · Use fit-for-purpose statistics, data visualization, predictive tools, and in silico / AI-enabled approaches to strengthen experimental design, molecular and material understanding, stability assessment, and biopharmaceutical risk evaluation.
- · Collaborate closely with Research, DMPK, Drug Safety, Process Chemistry, Formulation Development, and other partners as appropriate.
- · Provide scientific oversight of CROs and external laboratories, including study design, protocol / report review, progress monitoring, data evaluation, and resolution of technical issues.
- · Prepare and present study plans, technical reports, risk assessments, scientific recommendations, and development documentation for internal and external partners.
- · Contribute characterization content and scientific justification for regulatory documents and responses as appropriate to project phase and role.
- · Lead or contribute to initiatives that improve scientific quality, productivity, consistency, knowledge reuse, and technical capabilities across the organization.
- · Recognized as a technical expert across Pharm Sci functions
- · Serve as a technical resource or mentor for junior staff and leverage expertise in laboratory technology as a functional resource/trainer
この求人は、武田薬品工業株式会社の採用ページの内容をAIが読み取って整理したものです。応募の前に採用ページの原文を確かめてください。データの集め方企業サイト
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職種と勤務地が似ている求人神奈川県の研究職（応用研究員） 206件
神奈川県の研究職（応用研究員）の求人をすべて見る（206件）募集元の採用ページから応募できます
応募は武田薬品工業株式会社の採用ページで受け付けています。このページは採用ページの掲載内容をもとに構成しているため、最新の応募条件は募集元でご確認ください。
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