Bioassay Scientist - Cell-Based & Flow Cytometry

Eurofins; St. Louis (MO); On-site; USD 42,000 - 64,000; Full time

Benefits offered by this job

Medical, dental & vision coverage

Life and disability insurance

Paid holidays and vacation

Job summary

Eurofins PSS in Chesterfield, MO is seeking a life sciences professional to develop, perform and troubleshoot cell-based expression assays and flow cytometry to support product testing.

You will contribute to assay development using molecular biology techniques, document data per GMP, and collaborate with cross-functional teams to ensure timely, accurate testing. 1–3 years of relevant experience and US work authorization are required.

Qualifications

• Authorization to work in the United States indefinitely without restriction or sponsorship.
• 1-3 years of relevant industrial experience.
• Hands-on experience with molecular and cell biology techniques such as in vitro expression assays, mammalian cell culture, cell-based assays and flow cytometry.
• Experience in GMP or GMP-like environments preferred.
• Strong attention to detail and adherence to good documentation practices.
• Candidates within a commutable distance of Chesterfield, MO are encouraged to apply.

Responsibilities

• Develop, perform, and troubleshoot in vitro expression assays and flow cytometry to support product testing.
• Support assay development through molecular biology techniques.
• Document and report laboratory data in accordance with GMP practices.
• Collaborate with cross-functional project teams to ensure timely, accurate testing.

Skills

Flow Cytometry

Mammalian Cell Culture

In Vitro Expression

Cell-based Assays

Aseptic Technique

Documentation Skills

Education

Bachelors or Masters in Life Sciences

Job description

Eurofins PSS in Chesterfield, MO is seeking a life sciences professional to develop, perform and troubleshoot cell-based expression assays and flow cytometry to support product testing.

You will contribute to assay development using molecular biology techniques, document data per GMP, and collaborate with cross-functional teams to ensure timely, accurate testing. 1–3 years of relevant experience and US work authorization are required.