Analytical Scientist: HPLC & Biotherapeutic Assays

Eurofins PSS Insourcing Solutions; St. Louis (MO); On-site; USD 52,000 - 76,000; Full time

Benefits offered by this job

Medical, Dental, Vision

Life and disability insurance

Paid holidays and vacation

Job summary

Eurofins USA PSS Insourcing Solutions seeks an analytical specialist to support biotherapeutic process development focusing on large molecules. You will work with UV-Vis, HPLC, and gel-based assays within a diverse team and contribute to advancing pharmaceutical research.

The candidate will handle SDS-PAGE, CGE analyses and maintain GMP-compliant documentation while leveraging Empower/OpenLabs software as needed.

Qualifications

• Authorization to work in the United States indefinitely without restriction or sponsorship.
• 1-2+ years of industry/academic experience with the following techniques; HPLC/SEC, Western Blotting, and gel-based assay.
• Bachelor's or Master's degree in Biological or Chemical Science.
• Candidates within a commutable distance of Chesterfield, MO are encouraged to apply.
• Preferred experience: protein immunoblotting, electronic lab notebooks and GMP documentation.

Responsibilities

• Provide analytical support to biotherapeutic process development teams.
• Work with UV-Vis spectroscopy, HPLC, and gel-based assays.
• Assist with SDS-PAGE and CGE analyses.
• Maintain GMP-compliant documentation and electronic notebooks as required.

Skills

HPLC

SEC

Western Blotting

SDS PAGE

CGE

Gel-based assay

pH Appearance

Empower/OpenLabs

Education

Bachelor's degree in Biological or Chemical Science

Master's degree in Biological or Chemical Science

Tools

SOLO VPE

Empower/OpenLabs Software

Job description

Eurofins USA PSS Insourcing Solutions seeks an analytical specialist to support biotherapeutic process development focusing on large molecules. You will work with UV-Vis, HPLC, and gel-based assays within a diverse team and contribute to advancing pharmaceutical research.

The candidate will handle SDS-PAGE, CGE analyses and maintain GMP-compliant documentation while leveraging Empower/OpenLabs software as needed.