{"schemaVersion":"jobsearcher.job.v1","id":"bfb0335bed56cb6f388d11bf","url":"https://jobsearcher.com/jobs/bfb0335bed56cb6f388d11bf","canonicalUrl":"https://jobsearcher.com/jobs/bfb0335bed56cb6f388d11bf","title":"Senior Manager Analytical Development","description":"Senior Manager Analytical Development – LundbeckLocation: Bothell, WA, USPosted on: June 04, 2026Description:The characterization team includes analytical leads supporting Lundbeck biologics programs, and this role will also serve as an analytical lead as needed. This role will support development programs through execution of analytical strategies, including Critical Quality Attribute (CQA) identification and assessment.The successful candidate will have demonstrated leadership in analytical characterization of biologics, including a strong familiarity with the use of mass spectrometry as applied to biologics. Knowledge of protein biochemistry, enzymology, chromatography, N- and O-linked glycosylation, cell biology, biophysical characterization, and proteomics as they pertain to biologics will also be beneficial.This role operates within a matrixed team structure, contributing to management of the Potency team in Analytical Development.ESSENTIAL FUNCTIONSManage and develop a team of scientists, including coaching, mentoring, and performance managementDirectly contribute to experimental design, data analysis, troubleshooting, and interpretation of mass spectrometry dataProvide hands-on technical expertise in LC-MS-based characterization of biologics, including intact mass, peptide mapping, PTMs, sequence variant, HCP, and glycosylation analysisDesign, develop, and implement analytical methods for biologics characterization and routine testingServe as an analytical lead for biologics programs as needed, contributing to analytical strategy within cross-functional CMC teamsContribute to CQA identification, risk assessment, and characterization activitiesLead and execute characterization, comparability, and forced degradation studiesAuthor and review methods, protocols, reports, and regulatory documentationCollaborate closely with cross-functional teams to support development activities and timelinesOperate effectively within a matrix organization, supporting shared resourcesProvide administrative matrix management for assigned potency team members, including performance input and formal reviews, in alignment with potency scientific leadershipSupport transfer of analytical methods to external labs and review data as neededIdentify and implement improvements to analytical workflows and technologies as appropriateREQUIRED EDUCATION, EXPERIENCE and SKILLS:PhD in Biochemistry, Chemistry, Biological Science, or related field with a minimum of 5+ years relevant experienceExperience building high-performing teamsProven ability to manage performance, provide feedback, and drive accountabilityExperience managing or mentoring scientists while remaining technically hands-onExperience serving as an analytical lead or contributing to CMC teamsWorking knowledge of Critical Quality Attributes (CQAs) and characterization strategiesDeep expertise in mass spectrometry for biologics (intact mass, peptide mapping, PTM analysis)Strong understanding of biologics characterization and analytical method developmentExperience working in a matrixed organization is preferredStrong communication and collaboration skillsPREFERRED EDUCATION, EXPERIENCE AND SKILLS:Knowledge of biologics CMC development from pre-clinical through clinical to commercializationExperience in supporting regulatory submissionsExperience using mass spectrometry for identification and quantification of sequence variants (e.g., misincorporation), host cell proteins and N-glycan analysis/mappingPrior Leadership training would be beneficialTRAVEL:Willingness/Ability to travel up to 10% domestically and/or internationally.The 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: $170,000 - $190,000 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.Why LundbeckLundbeck 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.Lundbeck 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.Lundbeck 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. Lundbeck participates in E-Verify. 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This role will support development programs through execution of analytical strategies, including Critical Quality Attribute (CQA) identification and assessment.The successful candidate will have demonstrated leadership in analytical characterization of biologics, including a strong familiarity with the use of mass spectrometry as applied to biologics. Knowledge of protein biochemistry, enzymology, chromatography, N- and O-linked glycosylation, cell biology, biophysical characterization, and proteomics as they pertain to biologics will also be beneficial.This role operates within a matrixed team structure, contributing to management of the Potency team in Analytical Development.ESSENTIAL FUNCTIONSManage and develop a team of scientists, including coaching, mentoring, and performance managementDirectly contribute to experimental design, data analysis, troubleshooting, and interpretation of mass spectrometry dataProvide hands-on technical expertise in LC-MS-based characterization of biologics, including intact mass, peptide mapping, PTMs, sequence variant, HCP, and glycosylation analysisDesign, develop, and implement analytical methods for biologics characterization and routine testingServe as an analytical lead for biologics programs as needed, contributing to analytical strategy within cross-functional CMC teamsContribute to CQA identification, risk assessment, and characterization activitiesLead and execute characterization, comparability, and forced degradation studiesAuthor and review methods, protocols, reports, and regulatory documentationCollaborate closely with cross-functional teams to support development activities and timelinesOperate effectively within a matrix organization, supporting shared resourcesProvide administrative matrix management for assigned potency team members, including performance input and formal reviews, in alignment with potency scientific leadershipSupport transfer of analytical methods to external labs and review data as neededIdentify and implement improvements to analytical workflows and technologies as appropriateREQUIRED EDUCATION, EXPERIENCE and SKILLS:PhD in Biochemistry, Chemistry, Biological Science, or related field with a minimum of 5+ years relevant experienceExperience building high-performing teamsProven ability to manage performance, provide feedback, and drive accountabilityExperience managing or mentoring scientists while remaining technically hands-onExperience serving as an analytical lead or contributing to CMC teamsWorking knowledge of Critical Quality Attributes (CQAs) and characterization strategiesDeep expertise in mass spectrometry for biologics (intact mass, peptide mapping, PTM analysis)Strong understanding of biologics characterization and analytical method developmentExperience working in a matrixed organization is preferredStrong communication and collaboration skillsPREFERRED EDUCATION, EXPERIENCE AND SKILLS:Knowledge of biologics CMC development from pre-clinical through clinical to commercializationExperience in supporting regulatory submissionsExperience using mass spectrometry for identification and quantification of sequence variants (e.g., misincorporation), host cell proteins and N-glycan analysis/mappingPrior Leadership training would be beneficialTRAVEL:Willingness/Ability to travel up to 10% domestically and/or internationally.The 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: $170,000 - $190,000 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.Why LundbeckLundbeck 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.Lundbeck 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.Lundbeck 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. Lundbeck participates in E-Verify. J-18808-Ljbffr","datePosted":"2026-10-20T15:38:54.388Z","dateModified":"2026-10-20T15:38:54.388Z","hiringOrganization":{"@type":"Organization","name":"Glycodata","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Bothell","addressRegion":"WA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"bfb0335bed56cb6f388d11bf"},"url":"https://jobsearcher.com/jobs/bfb0335bed56cb6f388d11bf"}}