Pr. Bioassay Scientist

Eurofins BioPharma Product Testing North America

Columbia Township (MO)

On-site

USD 90,000 - 130,000

Full time

14 days+

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Benefits offered by this job

Comprehensive medical coverage

Dental and vision options

Life and disability insurance

401(k) with company match

Paid vacation and holidays

Job summary

A leading life sciences company located in Columbia Township, MO, is seeking a Scientist for its Biotech department. The ideal candidate will have extensive experience in cGMP laboratories and be proficient in method establishment and validations using ELISAs. Responsibilities include designing and executing complex experiments, analyzing data, and mentoring junior staff. Excellent full-time benefits include comprehensive medical coverage, 401(k), and paid vacation. The role offers a collaborative environment with a focus on quality and timely delivery.

Qualifications

5 years of experience in a cGMP laboratory with a Bachelor’s degree.
3 years of experience in a cGMP laboratory with a Master’s degree.
1 year of experience in a cGMP laboratory with a PhD.

Responsibilities

Design and perform experiments according to regulatory requirements.
Perform method establishment and validations.
Analyze data and communicate results effectively.
Train and mentor junior staff.
Utilize LIMS proficiently.

Skills

cGMP laboratory experience

Data analysis

Method establishment

Training and mentoring

LIMS

data analysis

train & mentor staff

Education

Bachelor’s degree in chemistry, biochemistry, or biology

Master’s degree

PhD

Tools

Molecular Devices Softmax Pro

Laboratory Information Management System (LIMS)

Job 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.

Job Description

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

Additional Information

Position is full-time, working Monday-Friday, 8:00 a.m.-4:30 p.m., plus any additional hours as needed. Candidates currently living within commutable distance to Columbia, MOare encouraged to apply.

What we Offer:

Excellent full-time benefits including