Senior Bioconjugate Process Development Scientist

Biopharma Careers

Thousand Oaks (CA)

On-site

USD 158,000 - 213,000

Full time

4 days ago
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Benefits offered by this job

Retirement plan
Stock-based incentives
Generous time-off

Job summary

Amgen is seeking a Senior Principal Scientist in Bioconjugates within the Process Development group at the Thousand Oaks campus. You will lead a multidisciplinary team to develop efficient manufacturing processes for bioconjugates, including ADCs, driving technology innovation and manufacturing readiness for clinical to late-stage programs.

The role emphasizes people-centered leadership, deep bioconjugation expertise, and collaboration across functions to enable regulatory filings and technology

Qualifications

  • Doctorate degree (PhD, PharmD or MD) with 3+ years of scientific experience.
  • Master's degree with 6+ years of scientific experience.
  • Bachelor's degree with 8+ years of scientific experience.

Responsibilities

  • Lead multidisciplinary project teams to develop sustainable bioconjugate manufacturing processes across clinical stages.
  • Drive bioconjugation technology innovation and process optimization.
  • Support cGMP manufacturing and technology transfer to GMP facilities.
  • Develop strategies to ensure process performance via understanding, modeling and characterization.
  • Ensure timely completion of project deliverables and regulatory filings.
  • Provide cross-functional collaboration and regulatory document support.
  • Act as technical expert and stay current in bioconjugation manufacturing.

Skills

Bioconjugation
Team leadership
Process development
Regulatory understanding

Education

PhD/MD/PharmD
Masters
Bachelor

Job description

Amgen is seeking a Senior Principal Scientist in Bioconjugates within the Process Development group at the Thousand Oaks campus. You will lead a multidisciplinary team to develop efficient manufacturing processes for bioconjugates, including ADCs, driving technology innovation and manufacturing readiness for clinical to late-stage programs.

The role emphasizes people-centered leadership, deep bioconjugation expertise, and collaboration across functions to enable regulatory filings and technology

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