About this role
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 independentlyGuide and mentor junior staff to successfully complete projects and grow technical knowledgeDo independent research into regulatory trends and technical advancesBe a technical resource for internal problems throughout Columbia BPTProvide support for corporate initiatives through BPT networkProvide coverage for management when neededDocument testing, observations, deviations, and results clearly and completely, and in compliance with regulatory requirements – striving to minimize errorsUnderstand and perform calculations as required by test methodsUnderstand and utilize computers for information access, calculations, and report preparationRead and understand analytical procedures (compendial and client supplied) and internal SOP’sAssist with onboarding new instrumentation, including performing/reviewing IQ/OQ/PQ data or qualificationsProvide consultation for clientsDemonstrate technical writing skills and complete investigations independentlyDemonstrate leadership qualities including - Effective communication - Display confidence - Demonstrate motivation and take initiative to Follow through on assignmentsProcess/review data, generate/review reports, and evaluate dataSuggest and implement lab improvements or modify existing processes to maximize quality and productivity; support and drive LEAN initiativesSupport or identify speaking or publishing opportunities and assist with driving to publication or presentationPerforms 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 laboratoryAuthorization to work in the U.S. without restriction or sponsorshipThe Ideal Candidate Would Possess:
Previous experience working in a CRO/CDMO adhering to cGMP regulationsAbility to conduct work efficiently, analyze data to ensure accuracy and report quality data.Industrial experience with method establishment and cGMP validations are highly desirableGood 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 optionsLife and disability insurance401(k) with company matchPaid vacation and holidaysEurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.