Eurofins USA BioPharma Services
Job Summary
Eurofins BPT-Columbia is looking for a
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
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.
Qualifications Minimum Qualifications
Bachelor’s degree in chemistry, biochemistry, or biology required
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.
Good problem solving, time management, communication, and interpersonal skills.
Industrial experience with method establishment and cGMP validations are highly desirable
Additional Information Position is full-time, Monday-Friday, 8:00 a.m.-4:30 p.m. with additional hours, as needed.
Candidates currently living within a commutable distance of Columbia, MO are encouraged to apply.
Benefits
Comprehensive medical coverage,
Life and disability insurance,
401(k) with company match,
Paid holidays and vacation,
Dental and vision options.
Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.
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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
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.
Qualifications Minimum Qualifications
Bachelor’s degree in chemistry, biochemistry, or biology required
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.
Good problem solving, time management, communication, and interpersonal skills.
Industrial experience with method establishment and cGMP validations are highly desirable
Additional Information Position is full-time, Monday-Friday, 8:00 a.m.-4:30 p.m. with additional hours, as needed.
Candidates currently living within a commutable distance of Columbia, MO are encouraged to apply.
Benefits
Comprehensive medical coverage,
Life and disability insurance,
401(k) with company match,
Paid holidays and vacation,
Dental and vision options.
Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.
#J-18808-Ljbffr