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.