Bioprocess Transfer Engineer – Scale-Up & Tech Transfer

Amgen SA

Thousand Oaks, Northern (CA, KY)

Hybrid

USD 121,000 - 190,000

Full time

2 days ago
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Benefits offered by this job

Stock benefits
Retirement plan
Medical insurance
Life & disability insurance
Annual bonus
Flexible work models

Job summary

Amgen is seeking an Engineer to transfer purification drug substance processes into manufacturing, optimize bioprocess scalability, and support tech transfers between sites. The role includes data analysis, process monitoring, and on-the-floor support for scale-up in a GMP environment.

Requires a Master’s degree in Chemical/Biochemical/Biomedical Engineering or related field and two years of engineering experience, with knowledge of JMP, SIMCA, DeltaV, and PI Vision.

Qualifications

  • Master’s degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering, or related field plus two years in engineering or related occupation.
  • Experience with technology transfer into commercial facilities and data analysis using JMP/Microsoft Office.
  • Familiarity with PPQ/Process Validation and GMP settings.

Responsibilities

  • Transfer purification drug substance processes from lab to manufacturing facilities.
  • Support tech transfers between partner sites via Make-a-Batch discussions.
  • Provide on-the-floor technical support for scale-up and transfer of process tech.
  • Perform data trending and statistical process analysis.
  • Contribute to deviations, CAPAs, and change controls.

Skills

Technology transfer
Data analysis
Root cause analysis
Process troubleshooting
Cross-functional collaboration

Education

Master’s degree in Chemical Engineering or related field

Tools

JMP
Microsoft Office
SIMCA
DeltaV
PI Vision

Job description

Amgen is seeking an Engineer to transfer purification drug substance processes into manufacturing, optimize bioprocess scalability, and support tech transfers between sites. The role includes data analysis, process monitoring, and on-the-floor support for scale-up in a GMP environment.

Requires a Master’s degree in Chemical/Biochemical/Biomedical Engineering or related field and two years of engineering experience, with knowledge of JMP, SIMCA, DeltaV, and PI Vision.

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