{"id":2269854,"url":"https://alion.io/job/lundbeck-senior-scientist-formulation-development","title":"Senior Scientist, Formulation Development","company":{"id":1772610,"name":"Lundbeck","domain":"lundbeck.com","url":"https://alion.io/company/lundbeck-com","size_band":null,"is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"SuccessFactors","truth_index":null},"role":"Science & Research","role_family":"Science & Research","seniority":"senior","employment_type":null,"work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Washington, United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":{"min":160000,"max":180000,"currency":"USD","period":"year","gross":null,"usd_annual":180000},"salary_estimate":null,"experience_years_min":12,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"ChatGPT","optional":true}],"status":"live","first_seen_at":"2026-10-11T07:23:38Z","employer_posted_date":"2026-10-11","last_verified_at":"2026-10-12T03:42:18Z","board_verified":true,"closed_at":null,"days_open":1,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":1},"description":"Do you want to join a team where the mission is meaningful, the challenges are complex, and you can directly see the results of your hard work? Lundbeck Seattle BioPharmaceuticals (Lu-SBP), located in Bothell, Washington, is the Process Development Center of Excellence for Biologics within the global Lundbeck CMC organization. Since integrating into Lundbeck in October 2019, Lu-SBP has supported commercial launch of Lundbeck’s first biologic product (Vyepti) and advancement of a growing biologics pipeline in collaboration with our Copenhagen-based Process Science & Validation Team. The Lu-SBP team leads and supports the development of new product candidates from cell line development through commercial validation of Drug Substance and Drug Product manufacturing processes. Join us on our journey to advance brain health and transform lives.\nPOSITION SUMMARY\nLundbeck Seattle's Center of Excellence located in Bothell, Washington is seeking a highly motivated and experienced Senior Scientist to join the Formulation Development team.\nThe successful candidate will possess extensive knowledge and industrial experience in biologic drug product formulation development, with expertise in developing stable protein formulations to support clinical and late-stage development. The candidate will demonstrate a strong understanding of protein stability, degradation mechanisms, formulation optimization, and drug product development to advance therapeutic biologics from early development through commercialization.\nThe ability to maintain scientific excellence, independently drive complex development activities, meet project timelines, and effectively influence cross-functional stakeholders is essential. The successful candidate will serve as a Subject Matter Expert (SME) in formulation development, collaborate closely with internal development teams, contribute to regulatory submissions, and represent Formulation Development on multidisciplinary project teams.\nESSENTIAL FUNCTIONS:\nDevelop robust formulations for biologic drug products, including liquid formulations and, when appropriate, lyophilized dosage forms.\nDesign, execute, and interpret formulation screening studies using statistical Design of Experiments (DOE) methodologies and software such as JMP.\nEvaluate protein physical and chemical stability using a broad range of analytical techniques and collaborate closely with Analytical Development to characterize degradation pathways.\nLead in-use compatibility studies to support clinical and commercial administration\nManage any out-sourced formulation development activities.\nAuthor and review formulation development reports, protocols, technical documents, and regulatory documentation supporting programs from IND through BLA submissions.\nPresent scientific data and project updates to cross-functional teams and senior management.\nCollaborate closely with Upstream, Downstream, Analytical Development, Quality, Regulatory Affairs, Manufacturing, and external partners to advance project objectives.\nIdentify opportunities to improve formulation development workflows through implementation of new technologies and innovative approaches.\nMaintain high standards of laboratory safety, documentation, and data integrity.\nREQUIRED EDUCATION, EXPERIENCE AND SKILLS:\nPh.D. with 5+ years of relevant experience in the biopharmaceutical industry, or M.S. with 10+ years, or B.S. with 12+ years, or equivalent combination of education and experience.\nDemonstrated expertise in biologic drug product formulation development.\nStrong understanding of protein structure, stability, aggregation mechanisms, and degradation pathways.\nExperience designing and executing high-throughput formulation screening studies using DOE.\nHands-on experience with analytical characterization techniques including SEC-HPLC, IEX-HPLC, DLS, MFI or HIAC, and related protein characterization methods.\nDemonstrated ability to independently manage laboratory studies, analyze complex datasets, and accurately document results.\nStrong scientific problem-solving, communication, and collaboration skills.\nPREFERRED EDUCATION, EXPERIENCE AND SKILLS:\nExperience with lyophilized biologic drug products and lyophilization process development is desirable.\nExperience supporting commercial or late-stage biologics development.\nStrong experience and skills working with AI such as Chat GPT.\nWorking knowledge of JMP or equivalent statistical software.\nExperience authoring and reviewing CMC sections for regulatory submissions (IND, BLA, MAA).\nFamiliarity with GMP manufacturing and Quality systems.\nStrong scientific writing skills.\nTRAVEL\nDomestic and international travel up to 10% may be required\nThe range displayed is specifically for those potential hires who will work or reside in the state of Washington, if selected for this role, and may vary based on various factors such as the candidate’s qualifications, skills, competencies, and proficiency for the role. Salary Pay Range: $160,000 - $180,000 and eligibility for a 15% bonus target based on company and individual performance, and eligibility to participate in the company’s long-term incentive plan. Additional benefits for this position include flexible paid time off (PTO), health benefits to include Medical, Dental and Vision and company match 401k. Additional benefits information can be found on our site. Applications accepted on an ongoing basis.#LI-LM1\nWhy Lundbeck\nLundbeck offers a robust and comprehensive benefits package to help employees live well and protect their health, family, and everyday life. Information regarding our benefit offering can be found on the U.S. career site.\nLundbeck is committed to working with and providing reasonable accommodations to disabled veterans and other individuals with disabilities during our employment application process. If, because of a disability, you need a reasonable accommodation for any part of the application process, please visit the U.S. career site.\nLundbeck is proud to be an equal opportunity workplace. We are committed to equal employment opportunity regardless of race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status, and any other characteristic protected by law, rule, or regulation. 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