Biologics Downstream Process Scientist I

Lundbeck A/S, H

Bothell (WA)

On-site

USD 135,000 - 155,000

Full time

5 days ago
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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

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.

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