Cell and Gene Therapy Scientist

Eurofins USA BioPharma Services

Cell and Gene Therapy Scientist

Columbia, MO
Full Time
Paid
  • Responsibilities

    Job Description

    _ Job Summary:_ Eurofins BPT-Columbia is looking for a **Senior Scientist ****** to join our Biologics Raw Materials team located in Columbia, Missouri. This individual will be a subject matter expert in testing Raw Materials used in Cell and Gene Therapy applications. The successful candidate will perform method establishment and validations under cGMP guidelines on a diverse set of methods including, HPLC, GC, Amino Acid Analysis, Mass Spectroscopy and FTIR. Ability to analyze data and effectively communicate results. Ability to complete work in an agreed upon timeline. Train team upon completion of method establishment and validation.

    Responsibilities include (but are not limited to):

    • Designing, carrying out, and performing simple and complex experiments and procedures in accordance with all applicable regulatory (e.g. DEA, EPA, FDA, FIFRA, OECD, etc.) requirements as defined by protocol, method, and standard operating procedures (SOPs).
    • Perform method establishment and validations on a diverse set of methods including HPLC, GC, Amino Acid Analysis, Mass Spectroscopy, and FTIR.
    • Analyze data with software including Empower and effectively communicate results.
    • Train and mentor junior staff.
    • Utilize laboratory information management system (LIMS) with proficiency.
    • Is able to utilize equipment, facilities, and personnel to produce sound scientific results in a timely fashion for Eurofins clients.
    • Adheres to schedule according to Eurofins or contracting organization’s timetable and establishes daily or weekly routines necessary to ensure on-time delivery.
  • Qualifications

    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 1+ years of experience working in a cGMP laboratory
    • Industrial experience with method establishment and cGMP validations are highly desirable
    • 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.
    • Good problem solving, time management, communication, and interpersonal skills.

    Additional Information

    The position is full-time, Monday-Friday, 8am-4:30pm, with overtime as needed. Candidates within a commutable distance of Columbia, MO are encouraged to apply.

    • 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

    To learn more about Eurofins, please explore our websitewww.eurofinsus.com.

    Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.