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
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.
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.