Principal Scientist, Downstream Process Innovation

Catalent

Madison (WI)

On-site

USD 150,000 - 210,000

Full time

2 days ago
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Benefits offered by this job

Day-one medical coverage
401(k) with match
Tuition reimbursement
Paid time off

Job summary

Catalent is seeking a Principal Scientist in Process Development – Downstream to lead upstream/downstream activities for biologics programs at our Madison site. The role blends scientific leadership with client-facing project management, overseeing downstream processes across mAbs, multispecifics, and proteins.

Responsibilities include guiding chromatography, UF/DF, filtration, and viral clearance while driving technology transfer and cGMP readiness.

Qualifications

  • Ph.D. or advanced degree with extensive biologics development experience.
  • Strong track record in downstream development of mAbs and proteins.
  • Proven leadership of technical programs and client-facing activities.

Responsibilities

  • Provide scientific leadership for downstream program strategy and execution.
  • Design and optimize chromatography, UF/DF, viral clearance and filtration steps.
  • Lead technology transfer and scale-up for cGMP manufacturing readiness.
  • Partner with clients to align technical execution with program goals.
  • Mentor scientists and cross-functional teams toward project milestones.
  • Ensure GDP-compliant documentation and regulatory readiness.

Skills

Scientific leadership
Client-facing
Project management

Education

Ph.D. in Biotechnology or related
M.S. in a relevant field
B.S. in a relevant field

Tools

Chromatography
UF/DF
Filtration
Viral clearance
Cell removal

Job description

Catalent is seeking a Principal Scientist in Process Development – Downstream to lead upstream/downstream activities for biologics programs at our Madison site. The role blends scientific leadership with client-facing project management, overseeing downstream processes across mAbs, multispecifics, and proteins.

Responsibilities include guiding chromatography, UF/DF, filtration, and viral clearance while driving technology transfer and cGMP readiness.

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