Scientist I - Downstream Process Development

Lundbeck; Bothell (WA); Sur place; USD 135 000 - 155 000; Plein temps

Avantages offerts par ce poste

Bonus target 10%

Health benefits

401k with company match

Flexible PTO

Résumé du poste

Lundbeck in Bothell, WA seeks a Scientist I in Downstream Process Development to advance scalable purification workflows for therapeutic biologics across preclinical to late-stage programs.

You will design and execute studies in chromatography, UF/DF, depth filtration, and viral clearance, collaborating with upstream, analytical, and formulation teams, and supporting tech transfer and manufacturing processes.

Qualifications

• Bachelor’s degree with 8+ years in biopharma, or Master’s with 6+ years, or PhD with 0–2 years in biopharma
• Expertise in protein purification using chromatography and filtration techniques (UF/DF, depth filtration, viral inactivation/filtration)
• Ability to independently design scientifically rigorous experiments and interpret complex datasets
• Proficiency in Unicorn-based AKTA programming and result evaluation

Responsabilités

• Design, execute, and interpret downstream studies for clinical and commercial programs
• Lead chromatography, UF/DF, depth filtration, viral inactivation and viral filtration activities
• Develop scalable and robust purification processes addressing performance and robustness
• Prepare technical reports, development documents, and transfer protocols
• Collaborate across upstream, analytical, and formulation development groups

Connaissances

Downstream process development

Data analysis & interpretation

Scientific report writing

AKTA Unicorn programming

Formation

Bachelor’s degree in a relevant field (Biopharma)

Master’s degree in a relevant field

PhD in a related field

Outils

Unicorn

AKTA chromatography systems

Filtration systems

Description du poste

Scientist I - Downstream Process Development

Location:

Bothell, WA, US

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 analyzes 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 oursite (https://www.lundbeck.com/content/dam/lundbeck-com/americas/united-states/careers/Lundbeck_Benefits_Summary.pdf) . Applications accepted on an ongoing basis.

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 theU.S. career site (https://www.lundbeck.com/content/dam/lundbeck-com/americas/united-states/careers/Lundbeck_Benefits_Summary.pdf) .

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 theU.S. career site (https://www.lundbeck.com/us/careers/your-job/eeo-accommodations-policy) .

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 inE-Verify (https://www.lundbeck.com/content/dam/lundbeck-com/americas/united-states/careers/E-Verify_Participation_Poster_Eng_Es.pdf) .

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 careers, 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.

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.