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Sr. Scientist – Process Development

Avantor · Bridgewater, NJ

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Role summary

Senior Scientist – Process Development role at Avantor focuses on developing and optimizing mRNA manufacturing processes under limited supervision. The position involves designing scalable workflows, applying quality-by-design principles, troubleshooting technical challenges, and collaborating across functions to advance process understanding and manufacturability.

Where this listing comes from

This listing was compiled by RoleLantern from the employer's publicly available posting on Phenom, captured and rephrased by RoleLantern using automated (AI) tools on 2026-10-04 (originally posted 2026-09-28). It was not submitted or confirmed by the employer through RoleLantern. Details may be inaccurate, incomplete, outdated, or no longer available; please confirm with the employer's official posting before applying.

What they're looking for

  • Ph.D. in Molecular Biology, Biochemistry, Bioengineering, Chemical/Biochemical Engineering, Pharmaceutical Sciences, or Biotechnology
  • Minimum 5+ years industry experience in mRNA, RNA, nucleic acid, or biologics process development
  • Strong expertise in mRNA process development including DNA template generation, in vitro transcription, enzymatic processing, and purification
  • Hands-on experience with nucleic acid techniques, molecular biology methods, and scalable manufacturing processes
  • Knowledge of DOE, QbD, process characterization, scale-up, risk assessment, and CPP/CQA relationships
  • Ability to troubleshoot complex technical challenges and develop data-driven solutions
  • Excellent technical writing, presentation, and cross-functional communication skills

What you'll be doing

  • Design and optimize end-to-end mRNA manufacturing processes from DNA template through formulation interfaces
  • Develop robust workflows to improve yield, purity, quality, and manufacturability of mRNA products
  • Apply DOE, QbD, and statistical tools to establish relationships between process parameters and quality attributes
  • Collaborate with analytical teams to characterize mRNA quality attributes and process impurities
  • Author technical reports, protocols, risk assessments, and regulatory documentation supporting process development

Privacy & handoff

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What RoleLantern checked

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Date posted7 days ago
Last source check1 day ago
Salary listedNeeds clarity
Location clearClear
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