Upstream Bioprocess Group Lead - Senior Principal Scientist

Merck

Rahway (NJ)

On-site

USD 173,000 - 273,000

Full time

24 hours ago
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Benefits offered by this job

Medical, dental, vision
401(k) plan
Paid holidays
Career development

Job summary

Merck is seeking a Senior Principal Scientist in Biologics Process Research & Development with leadership of 3–5 scientists to shape and drive upstream bioprocess innovations. You will lead scalable cell culture processes, coordinate cross-functional teams, and contribute to regulatory filings for biologics.

A strong publication/presentation background is preferred. The role emphasizes mentorship, strategic project planning, and collaboration with academia and vendors to accelerate development

Qualifications

  • PhD with 10+ years or MS with 12+ years, or BS with 14+ years in relevant field.
  • Strong expertise in cell-culture process development for biologics and bioreactor scale-up.
  • Proven track record in upstream bioprocessing with publications/presentations.
  • Experience leading cross-functional/matrixed teams.
  • Knowledge of CMC development for biologics.

Responsibilities

  • Shape and drive innovation across the Biologics pipeline and strategy.
  • Lead development of scalable upstream processes for biologics in clinical stages.
  • Mentor and develop scientists; build a cohesive team in a matrix environment.
  • Collaborate with academia, industry, and vendors to adopt novel technologies.
  • Represent BPR&D as an upstream bioprocess expert in project teams.

Skills

Cell culture
Bioreactor scale-up
Process development
Regulatory filings
Project leadership
Cross-functional teamwork
Communication
Mentoring

Education

PhD in Chemical/Biochemical Engineering
MS in Chemical/Biochemical Engineering
BS in Chemical Engineering

Job description

Merck is seeking a Senior Principal Scientist in Biologics Process Research & Development with leadership of 3–5 scientists to shape and drive upstream bioprocess innovations. You will lead scalable cell culture processes, coordinate cross-functional teams, and contribute to regulatory filings for biologics.

A strong publication/presentation background is preferred. The role emphasizes mentorship, strategic project planning, and collaboration with academia and vendors to accelerate development

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