Scientist I

Lundbeck A/S, H; Bothell (WA); On-site; USD 135,000 - 155,000; Full time

Benefits offered by this job

Health benefits

401k match

Bonus target

Job summary

Lundbeck Seattle BioPharmaceuticals (Lu-SBP) in Bothell, WA seeks a Scientist I for Downstream Process Development. You will develop scalable purification processes for biologics across preclinical to late-stage development, collaborating with upstream, analytical, and formulation teams.

The role emphasizes chromatography, UF/DF, filtration, and viral clearance, with opportunities to drive process robustness and tech transfer to manufacturing. A strong experimental design approach is required.

Qualifications

• Bachelor’s degree with 8+ years in biopharmaceuticals, or Master’s with 6+ years, or PhD with 0–2 years.
• Deep knowledge of protein purification principles and practical execution including chromatography and filtration techniques.
• Ability to independently design scientifically rigorous experiments and interpret complex datasets.
• Experience with AKTA programming and result evaluation.

Responsibilities

• Designs, executes, and interprets downstream process development studies for clinical and commercial programs.
• Lead chromatography, UF/DF, depth filtration, viral inactivation, and viral filtration efforts.
• Apply experimental design to develop robust, scalable processes.
• Analyze data, identify trends and risks, and translate results into clear conclusions.
• Author development documents, reports, and presentations for teams and stakeholders.
• Collaborate with manufacturing and other technical functions to support tech transfer and scale-up.

Skills

Chromatography

UF/DF

Depth filtration

Viral inactivation

Viral filtration

AKTA programming

Education

Bachelor's degree

Master's degree

PhD

Tools

Unicorn AKTA

Job description

Scientist I - Downstream Process Development

Requisition ID: 8211

Location: Bothell, WA, US

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

The Scientist I is a part of the Downstream Process Development team. This collaborative team develops processes for therapeutic biologic candidates in preclinical, clinical, and late-stage development. The primary responsibility will be to develop scalable and robust purification processes that produce protein within targeted product quality profile for clinical and commercial scales. This individual plays a synergistic role within downstream group and will collaborate extensively with members of upstream, analytical and formulation development groups.

Essential Functions

• Designs, executes, and interprets complex downstream process development studies supporting clinical and commercial biologics programs.
• Serves as a subject matter expert in downstream processing, with particular emphasis on Chromatography, Ultrafiltration/diafiltration (UF/DF), Depth filtration, Viral inactivation and Viral filtration.
• Apply strong experimental design principles to develop efficient, scientifically rigorous studies that address process performance, robustness, and scalability.
• Independently analyses complex experimental datasets, identify trends and risks, and translate results into clear technical conclusions and recommendations.
• Authors and reviews technical reports, development documents, presentations, protocols, and other documentation supporting process development activities.
• Presents scientific strategy, experimental results, recommendations, and technical risks to project teams and senior stakeholders.
• Serves as the Downstream Process Development functional-area lead on cross-functional development programs.
• Partners with Manufacturing and other technical functions to support process scale-up and technology transfer to internal or external manufacturing facilities.
• Provides technical support during manufacturing implementation, including troubleshooting and resolution of process-related issues.
• Collaborates effectively across organizational and geographic boundaries while maintaining clear communication and strong follow-through.

Required Education, Experience, and Skills

• Bachelor’s degree and 8+ years’ experience in biopharmaceutical industry or Masters and 6 years’ experience, or PhD and 0-2 years’ experience or relevant combination of education and experience.
• Extensive knowledge of the scientific principles and practical execution of protein purification using column chromatography and filtration techniques including UF/DF, depth filtration, viral inactivation, and viral filtration.
• Demonstrated ability to independently design scientifically rigorous experiments and interpret complex datasets.
• Skilled in Unicorn-based AKTA programming and result evaluation.

Preferred Education, Experience, and Skills

• BS or advanced degree in Chemical Engineering, Biochemical Engineering, Bioengineering, Biotechnology, Biochemistry, or a related scientific or engineering discipline.
• Experience supporting late-stage process development, process characterization, validation readiness, or commercial process development.
• Familiarity with viral clearance for early and late-stage programs.
• Experience supporting technology transfer activities, including preparation of process descriptions, transfer documentation, risk assessments, and manufacturing support.
• Hands‑on experience with pilot‑scale downstream processing equipment and operations.
• Familiarity with process characterization, scale‑down model qualification, and establishment of proven acceptable ranges or process operating ranges.
• Experience supporting regulatory filings or responding to technical questions related to downstream process development.
• Demonstrated experience leading a functional area on a cross‑functional development program and/or leading complex technical project teams.
• Ability to effectively coordinate activities across multiple functions, communicate priorities, identify risks, and drive decisions.
• Excellent verbal and written communication skills, including the ability to communicate complex technical concepts to both technical and non‑technical audiences.
• Strong organizational and project‑management skills, with demonstrated ability to manage multiple priorities and deliverables.

Travel Requirements

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

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: $135,000 - $155,000 and eligibility for a 10% 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

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 .

About Lundbeck

At Lundbeck, our most important contribution is easing the burden of the millions of people living with brain disorders. Whether it is migraine, depression, or other brain disorders, patients, their carers, and society as a whole depend on us.

Through cutting edge science and strong partnerships, we develop and market some of the world’s leading treatments, expanding into neuro‑specialty and neuro‑rare from our strong legacy within psychiatry and neurology.

The brain health challenge is real. Our commitment is real. Our impact is real.