Bioassay Scientist
Eurofins
Columbia, MO (In Person)
Full-Time
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Job Description
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.2025, Eurofins generated total revenues of EUR € 7.296 billion, and has been among the best performing stocks in Europe over the past 20 years.
Job DescriptionJob 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 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.
QualificationsMinimum Qualifications:
Bachelor's degree in chemistry, biochemistry, or biology requiredAuthorization to work in the U.S. without restriction or sponsorshipThe Ideal Candidate Would Possess:
Previous experience working in aCRO/CDMO
adhering to cGMP regulationsAbility 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 desirableAdditional InformationPosition is full-time, Monday-Friday 8am-4:30pm, plus additional hours, as needed. Candidates within a commutable distance of Columbia, MO are encouraged to apply.
Excellent full time benefits includingComprehensive medical coverage, dental, and vision optionsLife and disability insurance401(k) with company matchPaid vacation and holidaysEurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.
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