Downstream Vaccine Adjuvant & LNP Process Engineer

Eurofins

West Point (PA)

On-site

USD 120,000 - 165,000

Full time

10 days ago
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Benefits offered by this job

Medical, dental, and vision options
Life and disability insurance
401(k) with company match
Paid vacation and holidays

Job summary

Eurofins USA PSS Insourcing Solutions is seeking a qualified engineer to join our West Point, PA team to advance vaccine adjuvant and LNP processes. The role focuses on lab-scale downstream processing and analytical testing, with a strong emphasis on GMP-compliant documentation.

You will collaborate with cross-functional teams to optimize unit operations, maintain meticulous records, and ensure strict safety and quality standards while contributing to the scalable production of vaccine

Qualifications

  • Bachelor's degree in Engineering with 8+ years of experience or advanced degree with corresponding experience.
  • Authorization to work in the United States indefinitely without sponsorship.
  • Experience with adjuvant and LNP process operations such as extrusion and filtration.
  • Strong computer, scientific, and organizational skills.

Responsibilities

  • Perform lab-scale downstream processing of vaccine adjuvant & LNP products and process intermediates.
  • Perform assays on adjuvant & LNP products, process intermediates, and related experimental samples using biochemical/analytical tests.
  • Prepare solutions/reagents.
  • Set-up process equipment for lab-scale experiments.
  • Maintain records and experimental results following good manufacturing practices (GMP).

Skills

Lab-scale processing
GMP documentation
Analytical testing
Strong communication

Education

Bachelor's degree in Engineering
Master's degree in Engineering
PhD in Engineering

Job description

Eurofins USA PSS Insourcing Solutions is seeking a qualified engineer to join our West Point, PA team to advance vaccine adjuvant and LNP processes. The role focuses on lab-scale downstream processing and analytical testing, with a strong emphasis on GMP-compliant documentation.

You will collaborate with cross-functional teams to optimize unit operations, maintain meticulous records, and ensure strict safety and quality standards while contributing to the scalable production of vaccine

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