Pr. Scientist

Columbia, MO, USA

Full-time

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.

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.

Responsibilities include (but are not limited to):

Perform routine, non-routine and complex analyses; instrumental analyses; including calibration and troubleshooting/repair of instruments independently

Guide and mentor junior staff to successfully complete projects and grow technical knowledge

Do independent research into regulatory trends and technical advances

Be a technical resource for internal problems throughout Columbia BPT

Provide support for corporate initiatives through BPT network

Provide coverage for management when needed

Document testing, observations, deviations, and results clearly and completely, and in compliance with regulatory requirements - striving to minimize errors

Understand and perform calculations as required by test methods

Understand and utilize computers for information access, calculations, and report preparation

Read and understand analytical procedures (compendial and client supplied) and internal SOP's

Assist with onboarding new instrumentation, including performing/reviewing IQ/OQ/PQ data or qualifications

Provide consultation for clients

Demonstrate technical writing skills and complete investigations independently

Demonstrate leadership qualities including - Effective communication - Display confidence - Demonstrate motivation and take initiative to Follow through on assignments

Process/review data, generate/review reports, and evaluate data

Suggest and implement lab improvements or modify existing processes to maximize quality and productivity; support and drive LEAN initiatives

Support or identify speaking or publishing opportunities and assist with driving to publication or presentation

Performs other duties as assigned

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, MO are encouraged to apply.

What we Offer:

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.