Do you want to be part of an inclusive team that works to develop innovative therapies for patients? Every day, we are driven to develop and deliver innovative and effective new medicines to patients and physicians. If you want to be part of this exciting work, you belong at Astellas! Astellas Pharma Inc. is a pharmaceutical company conducting business in more than 70 countries around the world. We are committed to turning innovative science into medical solutions that bring value and hope to patients and their families. Keeping our focus on addressing unmet medical needs and conducting our business with ethics and integrity enables us to improve the health of people throughout the world. For more information on Astellas, please visit our website at **www.astellas.com** . **The Role:** + Responsible for the regulated bioanalytical assay development, validation and implementation of bioanalytical methods in the quantification of human biospecimens from clinical studies across multiple therapeutic areas/assets to support decision making. + Work in cross functional capacity to obtain clinical sample results to inform program strategy and clinical trial decisions. **Responsibilities** + Serve as a subject matter expert for regulated bioanalysis across multiple modalities, and QA audits. + Serve as a bioanalytical lead in asset teams and clinical development for decision making (Go/No-go) from P0 through post marketing obligations. + Collaborate with stakeholders providing solutions to challenges and mitigating risk. + Manage the bioanalytical assay transfer/validation, data review, quality and conduct at external bioanalytical vendors and ensuring regulatory compliance. + Provide technical expertise and guidance over the assay life cycle. + Contribute to regulatory submission documentation i.e., INDs, IBs, NDAs/BLAs + Ability to collaborate cross functionally within the research organization and clinical development across all regions. + Lead the identification and application of new technology assessments and utilization in human clinical trials + Keep current with all regulatory guidelines and technical innovations. + Follow and influence relevant Standard Operating Procedures and current bioanalytical regulatory guidelines. **Required Qualifications** + Ph.D. in chemistry, biochemistry, molecular biology, immunology, cell biology, or other relevant field, with 5+yrs industry experience, or MS degree with minimum 8+ years industry experience in biopharma development with a primary focus on the development, validation of regulated bioanalytical methods supporting clinical development. + Working knowledge of bioanalytical method validation and sample analysis regulatory guidelines in all regions (ICH, FDA, EMA, PMDA, etc.) + Extensive experience in chromatography assays of small molecules and biologics + Exposure to work experience in assay validations for ligand binding assays a plus + Must be able to work under strict or accelerated timelines with ability to provide deliverables + A clear and organized approach to work activities, strong process driven mindset with creative problem + solving skills. Great attention to detail and a work ethic to deliver high quality results. + Skilled in preparing and presenting scientific presentations + Participate in process improvements and develop best practices for bioanalysis operations + Self-motivated, excellent team player with good communication skills + Travel is <30% + Other relevant responsibilities as assigned **Preferred Qualifications** + Experience with immunocapture mass spectrometric analyses (hybrid LBA-LC-MS/MS) of complex biologics **Work Environment:** + At Astellas we recognize the importance of work/life balance, and we are proud to offer a hybrid working solution allowing time to connect with colleagues at the office with the flexibility to also work from home. We believe this will optimize the most productive work environment for all employees to succeed and deliver. + Hybrid work from certain locations may be permitted in accordance with Astellas’ Responsible Flexibility Guidelines **Salary Range:** $119,000 - 170,000 (NOTE: Final salary could be more or less, based on experience) **Benefits:** + Medical, Dental and Vision Insurance + Generous Paid Time Off options, including Vacation, Sick time, plus national holidays including Heritage Days, and Summer and Winter Breaks + 401(k) match and annual company contribution + Company paid life insurance + Annual Corporate Bonus and Quarterly Sales Incentive for eligible positions + Long Term Incentive Plan for eligible positions + Referral bonus program _All qualified applicants will receive consideration for employment without regard to race, sex, color, religion, sexual orientation, gender identity, national origin, protected veteran status, or on the basis of disability._ \#LI-TR1 Category Translational and Biomedical Science Astellas is committed to equality of opportunity in all aspects of employment. EOE including Disability/Protected Veterans