Pr. Scientist

Eurofins•Columbia, MO

1d•Onsite

About The Position

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

Requirements

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

Nice To Haves

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.

Responsibilities

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