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Jobs at KBI Biopharma

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Associate Scientist I - AFS

  • KBI Biopharma

    • On-site
    • Boulder, CO

Upstream Process Development Associate I/II

  • KBI Biopharma

    • On-site
    • Durham, NC

Maintenance Technician II/III

  • KBI Biopharma

    • On-site
    • Durham, NC

Senior Computer Systems Validation Specialist

  • KBI Biopharma

    • On-site
    • Durham, NC

Downstream PD Research Associate I/II

  • KBI Biopharma

    • On-site
    • Durham, NC

Microbiology Specialist I

  • KBI Biopharma

    • On-site
    • Durham, NC

Materials Coordinator

  • KBI Biopharma

    • On-site
    • Durham, NC

EHSS Specialist III

  • KBI Biopharma

    • On-site
    • Durham, NC

LIMS Laboratory Administrator - Analytical Formulation Sciences

  • KBI Biopharma

    • On-site
    • Boulder, CO

Senior Engineer, Manufacturing Sciences

  • KBI Biopharma

    • On-site
    • Durham, NC

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Associate Scientist I - AFS

  • KBI Biopharma

  • Boulder, CO 80329
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On-site

$75,000 - 110,000/ Year

Bio-Pharma

Quality+1

  • Posted on:

Job Description

Summary

At KBI Biopharma, we are advancing science and accelerating breakthroughs. As a global leader in biopharmaceutical development and manufacturing, we empower life science companies to bring new medicines and vaccines to the world faster.

Associate Scientist/Scientist I position in a growing team that supports a variety of analytical testing in support of the manufacturing of biopharmaceutical products in a contract development and manufacturing space.

Responsibilities
  • Support in-process testing in support of the manufacturing of biopharmaceutical products
  • Perform cGMP testing on product release and stability programs.
  • Perform stability trending, provides support for troubleshooting and laboratory investigations.
  • Regularly exercises technical discretion in the execution and interpretation of experiments that contribute to project goals.
  • Ensure accurate and complete documentation of results via electronic notebook, technical documents, power point, etc.
  • Provide support for the review and approval of analytical test methods, study protocols and technical reports.
  • Adheres to all safety requirements and assures that departmental employees comply with required safety procedures.
  • Able to react to change productively and handle other essential tasks as assigned.
Qualifications
  • For Associate Scientist: Bachelor’s degree in a related field and 5+ years’ experience or Master’s degree with 3+ years’ experience.
  • For Scientist I: Bachelor’s degree in a related field and 6+ years' experience or Master’s degree and 5+ years' experience or PhD and 0+ years' experience
  • Experience with cGMP and biotechnology-derived product regulations a plus.
  • Good written and verbal communication skills
  • Good critical thinking and scientific skills, with a demonstrated ability to analyze, interpret, and clearly present complex data with conclusions.
Experience:

0-6 yrs

  • Skills:
  • CGMP
  • Analytical Testing
  • Stability Testing
  • Data Analysis
  • technical writing
  • troubleshooting
  • Laboratory investigations
  • Job Type:
  • Full-time
  • Shift Type:
  • 8 hour shift
  • Monday to Friday

Compensation

  • Benefits:
  • 401K Match
  • Medical, Dental, Vision
  • 401K
  • Additional:
  • Base Salary

Job ID:

CGXP_26_29105

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