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.

POSITION SUMMARY

Lundbeck Seattle's Center of Excellence located in Bothell, Washington is seeking a highly motivated and experienced Senior Scientist to join the Formulation Development team.

The 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.

The 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.

ESSENTIAL FUNCTIONS:

• Develop robust formulations for biologic drug products, including liquid formulations and, when appropriate, lyophilized dosage forms.

• Design, execute, and interpret formulation screening studies using statistical Design of Experiments (DOE) methodologies and software such as JMP.

• Evaluate protein physical and chemical stability using a broad range of analytical techniques and collaborate closely with Analytical Development to characterize degradation pathways.

• Lead in-use compatibility studies to support clinical and commercial administration

• Manage any out-sourced formulation development activities.

• Author and review formulation development reports, protocols, technical documents, and regulatory documentation supporting programs from IND through BLA submissions.

• Present scientific data and project updates to cross-functional teams and senior management.

• Collaborate closely with Upstream, Downstream, Analytical Development, Quality, Regulatory Affairs, Manufacturing, and external partners to advance project objectives.

• Identify opportunities to improve formulation development workflows through implementation of new technologies and innovative approaches.

• Maintain high standards of laboratory safety, documentation, and data integrity.

REQUIRED EDUCATION, EXPERIENCE AND SKILLS:

• Ph.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.

• Demonstrated expertise in biologic drug product formulation development.

• Strong understanding of protein structure, stability, aggregation mechanisms, and degradation pathways.

• Experience designing and executing high-throughput formulation screening studies using DOE.

• Hands-on experience with analytical characterization techniques including SEC-HPLC, IEX-HPLC, DLS, MFI or HIAC, and related protein characterization methods.

• Demonstrated ability to independently manage laboratory studies, analyze complex datasets, and accurately document results.

• Strong scientific problem-solving, communication, and collaboration skills.

PREFERRED EDUCATION, EXPERIENCE AND SKILLS:

• Experience with lyophilized biologic drug products and lyophilization process development is desirable.

• Experience supporting commercial or late-stage biologics development.

• Strong experience and skills working with AI such as Chat GPT.

• Working knowledge of JMP or equivalent statistical software.

• Experience authoring and reviewing CMC sections for regulatory submissions (IND, BLA, MAA).

• Familiarity with GMP manufacturing and Quality systems.

• Strong scientific writing skills.

TRAVEL

• Domestic and international travel up to 10% may be required

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Why Lundbeck

Lundbeck 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.