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Senior Scientist

Eurofins

Senior Scientist

full-timePosted: Jan 16, 2026

Job Description

Description

Job Summary: Eurofins BPT-Columbia is looking for a Senior 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.

Qualifications

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
  • Industrial experience with method establishment and cGMP validations are highly desirable
  • 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.

Additional Info

Position 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 including:

  • Comprehensive medical coverage, dental, and vision options.
  • Life and disability insurance
  • 401(k) with company match
  • Paid vacation and holidays

 

Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

Company Description

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

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.

Locations

  • Columbia, MO, United States

Salary

Estimated Salary Rangemedium confidence

80,000 - 140,000 USD / yearly

Source: ai estimated

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • method establishmentintermediate
  • cGMP validationsintermediate
  • ELISAsintermediate
  • multiplex ELISAs (ECL)intermediate
  • data analysis (Softmax Pro)intermediate
  • LIMS proficiencyintermediate
  • training and mentoringintermediate

Required Qualifications

  • Bachelor’s degree + 5 years cGMP lab experience OR Master’s + 3 years OR PhD + 1 year (experience)

Responsibilities

  • Perform method establishment and validations
  • Design and carry out experiments
  • Analyze data and communicate results
  • Train and mentor junior staff
  • Utilize LIMS
  • Adhere to schedule for on-time delivery

Benefits

  • general: comprehensive medical coverage
  • general: dental and vision options
  • general: life and disability insurance
  • general: 401(k) with company match
  • general: paid vacation and holidays

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Eurofins logo

Senior Scientist

Eurofins

Senior Scientist

full-timePosted: Jan 16, 2026

Job Description

Description

Job Summary: Eurofins BPT-Columbia is looking for a Senior 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.

Qualifications

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
  • Industrial experience with method establishment and cGMP validations are highly desirable
  • 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.

Additional Info

Position 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 including:

  • Comprehensive medical coverage, dental, and vision options.
  • Life and disability insurance
  • 401(k) with company match
  • Paid vacation and holidays

 

Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

Company Description

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

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.

Locations

  • Columbia, MO, United States

Salary

Estimated Salary Rangemedium confidence

80,000 - 140,000 USD / yearly

Source: ai estimated

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • method establishmentintermediate
  • cGMP validationsintermediate
  • ELISAsintermediate
  • multiplex ELISAs (ECL)intermediate
  • data analysis (Softmax Pro)intermediate
  • LIMS proficiencyintermediate
  • training and mentoringintermediate

Required Qualifications

  • Bachelor’s degree + 5 years cGMP lab experience OR Master’s + 3 years OR PhD + 1 year (experience)

Responsibilities

  • Perform method establishment and validations
  • Design and carry out experiments
  • Analyze data and communicate results
  • Train and mentor junior staff
  • Utilize LIMS
  • Adhere to schedule for on-time delivery

Benefits

  • general: comprehensive medical coverage
  • general: dental and vision options
  • general: life and disability insurance
  • general: 401(k) with company match
  • general: paid vacation and holidays

Target Your Resume for "Senior Scientist" , Eurofins

Get personalized recommendations to optimize your resume specifically for Senior Scientist. Takes only 15 seconds!

AI-powered keyword optimization
Skills matching & gap analysis
Experience alignment suggestions

Check Your ATS Score for "Senior Scientist" , Eurofins

Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.

ATS compatibility check
Keyword optimization analysis
Skill matching & gap identification
Format & readability score

Answer 10 quick questions to check your fit for Senior Scientist @ Eurofins.

Quiz Challenge
10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.