Skip to content

Downstream Process Scientist - Viral Vector Manufacturing

Eurofins BioPharma Product Testing · Spring House, PA

Posted November 10, 2026

Mid levelProductionGMPOn site
Pay not postedApply

Quick facts

Experience
0 to 2+ years, depending on education
Education
Bachelor's or Master's
Job type
Full-time
Schedule
Monday to Friday
Skills mentioned
GMP, Data integrity, Downstream processing, Chromatography (purification), Biologics, Procurement

Pulled from the ad below. The full ad has the details.

Job Description

This role is expected to perform experiments to support downstream process development activities for viral vectors manufacturing.

  • Execute Tangential Flow Filtration (TFF) operations, including system setup, processing, monitoring, and documentation
  • Support downstream processing activities, including Clarification, Nuclease Treatment, Fitler Screening, Sterile Filtration and AEX chromatography (both manual and AKTA-based operations)
  • Perform and support column packing activities
  • Capture, maintain, and document process parameters and analytical data within the project Master Data File
  • Assist with inventory management and the procurement of project supplies to ensure material availability and operational continuity
  • Record and analyze experimental data, verify data integrity and accuracy
  • Report/summarize findings to the project team
  • Write technical documents and main work records in electronic notebooks

Qualifications

Minimum Qualifications

  • Bachelor’s degree in life sciences or a related scientific discipline is required with 2+ years of direct Downstream experience, Masters degree with 0-2 years experience
  • Hands-on experience in purification of proteins or biologics is required
  • Broad knowledge in chromatography techniques and purification process development is required
  • Ability to document work accurately in notebooks, protocols, reports, and electronic systems
  • Strong scientific, organizational, communication, and attention-to-detail skills
  • Authorization to work in the United States indefinitely without restriction or sponsorship

Preferred Experience

  • GMP knowledge and experience working in a regulated laboratory environment.
  • Previous experience with Viral Vectors
  • Previous experience with transfer of a purification process to clinical and commercial GMP manufacturing is preferred

Additional Information

This position is Full-Time, Monday - Friday, 8:00 a.m. - 5:00 p.m . Candidates currently living within a commutable distance of Spring House, PA are encouraged to apply.

  • Excellent full-time benefits including comprehensive medical coverage, dental, and vision options
  • Life and disability insurance
  • 401(k) with company match
  • Paid vacation and holidays

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Source: Eurofins BioPharma Product Testing's career site. PharmoniQ shows this job as posted and links to the original. Check the employer's page for the latest details.