Bioassay Scientist - Sr. Scientist

Job Summary: Eurofins BPT-Columbia is looking for a Sr. Scientist to join our team located in Columbia, Missouri. This individual will be a subject matter expert in testing Drug Substances and Drug Products in the Biotech department. The successful candidate will perform method establishment and validations under cGMP guidelines on a diverse set of methods including, ELISAs, and multiplex ELISAs using electrochemiluminescence (ECL) methodologies. Ability to analyze data and effectively communicate results. Ability to complete work in an agreed upon timeline. Train team upon completion of method establishment and validation.
Responsibilities include (but are not limited to):
Designing, carrying out, and performing simple and complex experiments and procedures in accordance with all applicable regulatory (e.g. DEA, EPA, FDA, FIFRA, OECD, etc.) requirements as defined by protocol, method, and standard operating procedures (SOPs).
Perform method establishment and validations on a diverse set of methods including multiplex ELISAs using ECL platforms.
Analyze data with software including Molecular Devices Softmax Pro and effectively communicate results.
Train and mentor junior staff.
Utilize laboratory information management system (LIMS) with proficiency.
Is able to utilize equipment, facilities, and personnel to produce sound scientific results in a timely fashion for Eurofins clients.
Adheres to schedule according to Eurofins or contracting organization’s timetable and establishes daily or weekly routines necessary to ensure on-time delivery.
Minimum Qualifications:
Bachelor’s degree in chemistry, biochemistry, or biology and 5 years of experience working in a cGMP laboratory OR Master’s degree and 3 years of experience working in a cGMP laboratory OR PhD and minimum 1 year(s) of experience working in a cGMP laboratory
Authorization to work in the U.S. without restriction or sponsorship
The Ideal Candidate Would Possess:
Previous experience working in a CRO/CDMO adhering to cGMP regulations
Ability to conduct work efficiently, analyze data to ensure accuracy and report quality data.
Industrial experience with method establishment and cGMP validations are highly desirable
Good problem solving, time management, communication, and interpersonal skills.

Employment type
Full-time

Work arrangement
No